Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP310869.RAuPe2kiSXaNySPB4iK7p1_86Utho54H0m2VsZ92Tss5s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP310869.RAuPe2kiSXaNySPB4iK7p1_86Utho54H0m2VsZ92Tss5s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP310869.RAuPe2kiSXaNySPB4iK7p1_86Utho54H0m2VsZ92Tss5s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP310869.RAuPe2kiSXaNySPB4iK7p1_86Utho54H0m2VsZ92Tss5s130_provenance.
- NP310869.RAuPe2kiSXaNySPB4iK7p1_86Utho54H0m2VsZ92Tss5s130_assertion description "[A common polymorphism of TM at amino acid position 455 with an alanine (A) to valine (V) transition was previously reported to be associated cross-sectionally with acute myocardial infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP310869.RAuPe2kiSXaNySPB4iK7p1_86Utho54H0m2VsZ92Tss5s130_provenance.
- NP310869.RAuPe2kiSXaNySPB4iK7p1_86Utho54H0m2VsZ92Tss5s130_assertion evidence source_evidence_literature NP310869.RAuPe2kiSXaNySPB4iK7p1_86Utho54H0m2VsZ92Tss5s130_provenance.
- NP310869.RAuPe2kiSXaNySPB4iK7p1_86Utho54H0m2VsZ92Tss5s130_assertion SIO_000772 11245641 NP310869.RAuPe2kiSXaNySPB4iK7p1_86Utho54H0m2VsZ92Tss5s130_provenance.
- NP310869.RAuPe2kiSXaNySPB4iK7p1_86Utho54H0m2VsZ92Tss5s130_assertion wasDerivedFrom befree-2016 NP310869.RAuPe2kiSXaNySPB4iK7p1_86Utho54H0m2VsZ92Tss5s130_provenance.
- NP310869.RAuPe2kiSXaNySPB4iK7p1_86Utho54H0m2VsZ92Tss5s130_assertion wasGeneratedBy ECO_0000203 NP310869.RAuPe2kiSXaNySPB4iK7p1_86Utho54H0m2VsZ92Tss5s130_provenance.
- befree-2016 importedOn "2016-02-19" NP310869.RAuPe2kiSXaNySPB4iK7p1_86Utho54H0m2VsZ92Tss5s130_provenance.