Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP594154.RACHuaHJPXmli5_s5GgQfifKlDZBkUeetrFAY6R4mMIMU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP594154.RACHuaHJPXmli5_s5GgQfifKlDZBkUeetrFAY6R4mMIMU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP594154.RACHuaHJPXmli5_s5GgQfifKlDZBkUeetrFAY6R4mMIMU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP594154.RACHuaHJPXmli5_s5GgQfifKlDZBkUeetrFAY6R4mMIMU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP594154.RACHuaHJPXmli5_s5GgQfifKlDZBkUeetrFAY6R4mMIMU130_provenance.
- NP594154.RACHuaHJPXmli5_s5GgQfifKlDZBkUeetrFAY6R4mMIMU130_assertion wasGeneratedBy ECO_0000203 NP594154.RACHuaHJPXmli5_s5GgQfifKlDZBkUeetrFAY6R4mMIMU130_provenance.
- NP594154.RACHuaHJPXmli5_s5GgQfifKlDZBkUeetrFAY6R4mMIMU130_assertion wasDerivedFrom befree-20150227 NP594154.RACHuaHJPXmli5_s5GgQfifKlDZBkUeetrFAY6R4mMIMU130_provenance.
- NP594154.RACHuaHJPXmli5_s5GgQfifKlDZBkUeetrFAY6R4mMIMU130_assertion SIO_000772 15091109 NP594154.RACHuaHJPXmli5_s5GgQfifKlDZBkUeetrFAY6R4mMIMU130_provenance.
- NP594154.RACHuaHJPXmli5_s5GgQfifKlDZBkUeetrFAY6R4mMIMU130_assertion evidence source_evidence_literature NP594154.RACHuaHJPXmli5_s5GgQfifKlDZBkUeetrFAY6R4mMIMU130_provenance.
- NP594154.RACHuaHJPXmli5_s5GgQfifKlDZBkUeetrFAY6R4mMIMU130_assertion description "[In this prospective clinical study involving 141 participants, we used gene microarray technology to demonstrate that the eNOS gene intron-4 27-base pair variable number tandem repeat polymorphism (eNOS 27 VNTR) predicts susceptibility to intracranial aneurysm rupture, while the eNOS gene promoter T-786C single nucleotide polymorphism (eNOS T-786C SNP) predicts susceptibility to post-subarachnoid hemorrhage vasospasm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP594154.RACHuaHJPXmli5_s5GgQfifKlDZBkUeetrFAY6R4mMIMU130_provenance.