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<http://identifiers.org/ncbigene/51156> <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#NP141515.RAsnjiPsVs4_t1sJy4PinZCJIujU1Bio5npDr8P85_Xq0130_assertion> .
<http://linkedlifedata.com/resource/umls/id/C0042487> <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#NP141515.RAsnjiPsVs4_t1sJy4PinZCJIujU1Bio5npDr8P85_Xq0130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN244506aeab32e243e43259fb4742a2a3> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ncbigene/51156> <http://rdf.disgenet.org/nanopublications.trig#NP141515.RAsnjiPsVs4_t1sJy4PinZCJIujU1Bio5npDr8P85_Xq0130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN244506aeab32e243e43259fb4742a2a3> <http://semanticscience.org/resource/SIO_000628> <http://linkedlifedata.com/resource/umls/id/C0042487> <http://rdf.disgenet.org/nanopublications.trig#NP141515.RAsnjiPsVs4_t1sJy4PinZCJIujU1Bio5npDr8P85_Xq0130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN244506aeab32e243e43259fb4742a2a3> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_001122> <http://rdf.disgenet.org/nanopublications.trig#NP141515.RAsnjiPsVs4_t1sJy4PinZCJIujU1Bio5npDr8P85_Xq0130_assertion> .
<http://rdf.disgenet.org/nanopublications.trig#NP141515.RAsnjiPsVs4_t1sJy4PinZCJIujU1Bio5npDr8P85_Xq0130_assertion> <http://purl.org/dc/terms/description> "[Our study supports that the ZPI Arg67Stop nonsense polymorphism might be an independent genetic risk factor for venous thrombosis/polymorphism has slightly lower prevalence but similar thrombotic risk than the FV Leiden or prothrombin 20210A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/nanopublications.trig#NP141515.RAsnjiPsVs4_t1sJy4PinZCJIujU1Bio5npDr8P85_Xq0130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP141515.RAsnjiPsVs4_t1sJy4PinZCJIujU1Bio5npDr8P85_Xq0130_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#NP141515.RAsnjiPsVs4_t1sJy4PinZCJIujU1Bio5npDr8P85_Xq0130_provenance> .
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<http://rdf.disgenet.org/v2.1.0/void.ttl#lhgdn-20090331> <http://purl.org/pav/2.0/importedOn> "2009-03-31"^^<http://www.w3.org/2001/XMLSchema#date> <http://rdf.disgenet.org/nanopublications.trig#NP141515.RAsnjiPsVs4_t1sJy4PinZCJIujU1Bio5npDr8P85_Xq0130_provenance> .
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<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#NP141515.RAsnjiPsVs4_t1sJy4PinZCJIujU1Bio5npDr8P85_Xq0130_provenance> .
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