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<http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.nanopub.org/nschema#Nanopublication> <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_head> .
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<http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_provenance> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.nanopub.org/nschema#Provenance> <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_head> .
<http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_publicationInfo> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.nanopub.org/nschema#PublicationInfo> <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_head> .
<http://identifiers.org/ncbigene/1910> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16612> <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_assertion> .
<http://linkedlifedata.com/resource/umls/id/C0013080> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C7057> <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN02cd7c20a74e2e2a6feff12a0ab34b60> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ncbigene/1910> <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN02cd7c20a74e2e2a6feff12a0ab34b60> <http://semanticscience.org/resource/SIO_000628> <http://linkedlifedata.com/resource/umls/id/C0013080> <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN02cd7c20a74e2e2a6feff12a0ab34b60> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_001121> <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_assertion> .
<http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_assertion> <http://purl.org/dc/terms/description> "[Detection of the 178G/A polymorphism in only non-syndromic HSCR patients, provide further support for an important role of specific sequence variants in the EDNRB gene in the HSCR/Down's syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_assertion> <http://purl.org/ontology/wi/core#evidence> <http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_assertion> <http://semanticscience.org/resource/SIO_000772> <http://identifiers.org/pubmed/12628594> <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_assertion> <http://www.w3.org/ns/prov#wasDerivedFrom> <http://rdf.disgenet.org/v2.1.0/void.ttl#befree-20140225> <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_assertion> <http://www.w3.org/ns/prov#wasGeneratedBy> <http://purl.obolibrary.org/obo/eco.owl#ECO_0000203> <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_provenance> .
<http://rdf.disgenet.org/v2.1.0/void.ttl#befree-20140225> <http://purl.org/pav/2.0/importedOn> "2014-02-25"^^<http://www.w3.org/2001/XMLSchema#date> <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_provenance> .
<http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://purl.obolibrary.org/obo/eco.owl#ECO_0000212> <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_provenance> .
<http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://www.w3.org/2000/01/rdf-schema#comment> "Gene-disease associations inferred from text-mining the literature."@en <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_provenance> .
<http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://www.w3.org/2000/01/rdf-schema#label> "DisGeNET evidence - LITERATURE"@en <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA> <http://purl.org/dc/terms/created> "2014-10-02T12:36:30+02:00"^^<http://www.w3.org/2001/XMLSchema#dateTime> <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_publicationInfo> .
<http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA> <http://purl.org/dc/terms/rights> <http://opendatacommons.org/licenses/odbl/1.0/> <http://rdf.disgenet.org/nanopublications.trig#NP453608.RANBbSFNL8B4UUUSdSofsPrREiZhn9e1Q1KBMD7xDPusA130_publicationInfo> .
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