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<http://rdf.disgenet.org/nanopublications.trig#NP389722.RActXw4BpiEdJGPiopeisSiOm6CGKmGxkTXNFhdCkg0Lc> <http://www.nanopub.org/nschema#hasPublicationInfo> <http://rdf.disgenet.org/nanopublications.trig#NP389722.RActXw4BpiEdJGPiopeisSiOm6CGKmGxkTXNFhdCkg0Lc130_publicationInfo> <http://rdf.disgenet.org/nanopublications.trig#NP389722.RActXw4BpiEdJGPiopeisSiOm6CGKmGxkTXNFhdCkg0Lc130_head> .
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<http://identifiers.org/ncbigene/131566> <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#NP389722.RActXw4BpiEdJGPiopeisSiOm6CGKmGxkTXNFhdCkg0Lc130_assertion> .
<http://linkedlifedata.com/resource/umls/id/C0340068> <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#NP389722.RActXw4BpiEdJGPiopeisSiOm6CGKmGxkTXNFhdCkg0Lc130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN6d25e24fd3cd64cfd25f43a5c6614378> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ncbigene/131566> <http://rdf.disgenet.org/nanopublications.trig#NP389722.RActXw4BpiEdJGPiopeisSiOm6CGKmGxkTXNFhdCkg0Lc130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN6d25e24fd3cd64cfd25f43a5c6614378> <http://semanticscience.org/resource/SIO_000628> <http://linkedlifedata.com/resource/umls/id/C0340068> <http://rdf.disgenet.org/nanopublications.trig#NP389722.RActXw4BpiEdJGPiopeisSiOm6CGKmGxkTXNFhdCkg0Lc130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN6d25e24fd3cd64cfd25f43a5c6614378> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_001121> <http://rdf.disgenet.org/nanopublications.trig#NP389722.RActXw4BpiEdJGPiopeisSiOm6CGKmGxkTXNFhdCkg0Lc130_assertion> .
<http://rdf.disgenet.org/nanopublications.trig#NP389722.RActXw4BpiEdJGPiopeisSiOm6CGKmGxkTXNFhdCkg0Lc130_assertion> <http://purl.org/dc/terms/description> "[Among these variants, seven SNPs (rs1371687, rs7615856, rs828621, rs828618, rs828616, rs1062196, and rs8833) and one haplotype (DCBLD2-ht1) show associations with susceptibility to AERD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/nanopublications.trig#NP389722.RActXw4BpiEdJGPiopeisSiOm6CGKmGxkTXNFhdCkg0Lc130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP389722.RActXw4BpiEdJGPiopeisSiOm6CGKmGxkTXNFhdCkg0Lc130_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#NP389722.RActXw4BpiEdJGPiopeisSiOm6CGKmGxkTXNFhdCkg0Lc130_provenance> .
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<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#NP389722.RActXw4BpiEdJGPiopeisSiOm6CGKmGxkTXNFhdCkg0Lc130_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#NP389722.RActXw4BpiEdJGPiopeisSiOm6CGKmGxkTXNFhdCkg0Lc130_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#NP389722.RActXw4BpiEdJGPiopeisSiOm6CGKmGxkTXNFhdCkg0Lc130_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#NP389722.RActXw4BpiEdJGPiopeisSiOm6CGKmGxkTXNFhdCkg0Lc130_provenance> .
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