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<http://identifiers.org/ncbigene/1636> <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#NP123230.RAWPy2y8wUrOnWVd3xXL3_FKmcR3RlYB_Doc5D4-lgptM130_assertion> .
<http://linkedlifedata.com/resource/umls/id/C0020538> <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#NP123230.RAWPy2y8wUrOnWVd3xXL3_FKmcR3RlYB_Doc5D4-lgptM130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN084f7d84a8b2d4e2439ff3d2a40ec100> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ncbigene/1636> <http://rdf.disgenet.org/nanopublications.trig#NP123230.RAWPy2y8wUrOnWVd3xXL3_FKmcR3RlYB_Doc5D4-lgptM130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN084f7d84a8b2d4e2439ff3d2a40ec100> <http://semanticscience.org/resource/SIO_000628> <http://linkedlifedata.com/resource/umls/id/C0020538> <http://rdf.disgenet.org/nanopublications.trig#NP123230.RAWPy2y8wUrOnWVd3xXL3_FKmcR3RlYB_Doc5D4-lgptM130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN084f7d84a8b2d4e2439ff3d2a40ec100> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_001122> <http://rdf.disgenet.org/nanopublications.trig#NP123230.RAWPy2y8wUrOnWVd3xXL3_FKmcR3RlYB_Doc5D4-lgptM130_assertion> .
<http://rdf.disgenet.org/nanopublications.trig#NP123230.RAWPy2y8wUrOnWVd3xXL3_FKmcR3RlYB_Doc5D4-lgptM130_assertion> <http://purl.org/dc/terms/description> "[The present study suggests that none of the major genetic polymorphisms in the RAA system (angiotensinogen, angiotensin-converting enzyme, angiotensin II type 1 receptor, and aldosterone synthase) strongly influence the onset of essential hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/nanopublications.trig#NP123230.RAWPy2y8wUrOnWVd3xXL3_FKmcR3RlYB_Doc5D4-lgptM130_provenance> .
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<http://rdf.disgenet.org/nanopublications.trig#NP123230.RAWPy2y8wUrOnWVd3xXL3_FKmcR3RlYB_Doc5D4-lgptM130_assertion> <http://www.w3.org/ns/prov#wasGeneratedBy> <http://purl.obolibrary.org/obo/eco.owl#ECO_0000203> <http://rdf.disgenet.org/nanopublications.trig#NP123230.RAWPy2y8wUrOnWVd3xXL3_FKmcR3RlYB_Doc5D4-lgptM130_provenance> .
<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#NP123230.RAWPy2y8wUrOnWVd3xXL3_FKmcR3RlYB_Doc5D4-lgptM130_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#NP123230.RAWPy2y8wUrOnWVd3xXL3_FKmcR3RlYB_Doc5D4-lgptM130_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#NP123230.RAWPy2y8wUrOnWVd3xXL3_FKmcR3RlYB_Doc5D4-lgptM130_provenance> .
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