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<http://rdf.disgenet.org/nanopublications.trig#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_publicationInfo> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://www.nanopub.org/nschema#PublicationInfo> <http://rdf.disgenet.org/nanopublications.trig#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_head> .
<http://identifiers.org/ncbigene/368> <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#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_assertion> .
<http://linkedlifedata.com/resource/umls/id/C0010068> <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#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN7a377d59214bd5604e9568a474e1e349> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ncbigene/368> <http://rdf.disgenet.org/nanopublications.trig#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN7a377d59214bd5604e9568a474e1e349> <http://semanticscience.org/resource/SIO_000628> <http://linkedlifedata.com/resource/umls/id/C0010068> <http://rdf.disgenet.org/nanopublications.trig#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN7a377d59214bd5604e9568a474e1e349> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_001121> <http://rdf.disgenet.org/nanopublications.trig#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_assertion> .
<http://rdf.disgenet.org/nanopublications.trig#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_assertion> <http://purl.org/dc/terms/description> "[Mutations in the gene cause a rare, recessive genetic disease, pseudoxanthoma elasticum, while the loss of one ABCC6 allele is a genetic risk factor in coronary artery disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/nanopublications.trig#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_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#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_assertion> <http://semanticscience.org/resource/SIO_000772> <http://identifiers.org/pubmed/21039331> <http://rdf.disgenet.org/nanopublications.trig#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_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#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_assertion> <http://www.w3.org/ns/prov#wasGeneratedBy> <http://purl.obolibrary.org/obo/eco.owl#ECO_0000203> <http://rdf.disgenet.org/nanopublications.trig#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_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#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_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#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_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#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_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#NP424804.RANMnDlyF-v-Lz3Mur_T3cflMIdc8mUAIY57F8U5iOq9Q130_provenance> .
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