Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP20761.RAaVF8iALZUIKWOas0XSxt881bz04seizkoanA32iftkc130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP20761.RAaVF8iALZUIKWOas0XSxt881bz04seizkoanA32iftkc130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP20761.RAaVF8iALZUIKWOas0XSxt881bz04seizkoanA32iftkc130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP20761.RAaVF8iALZUIKWOas0XSxt881bz04seizkoanA32iftkc130_provenance.
- NP20761.RAaVF8iALZUIKWOas0XSxt881bz04seizkoanA32iftkc130_assertion description "[Three missense mutations associated with long QT syndrome and ventricular fibrillation are identified in the gene for MiRP1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20761.RAaVF8iALZUIKWOas0XSxt881bz04seizkoanA32iftkc130_provenance.
- NP20761.RAaVF8iALZUIKWOas0XSxt881bz04seizkoanA32iftkc130_assertion evidence source_evidence_curated NP20761.RAaVF8iALZUIKWOas0XSxt881bz04seizkoanA32iftkc130_provenance.
- NP20761.RAaVF8iALZUIKWOas0XSxt881bz04seizkoanA32iftkc130_assertion SIO_000772 10219239 NP20761.RAaVF8iALZUIKWOas0XSxt881bz04seizkoanA32iftkc130_provenance.
- NP20761.RAaVF8iALZUIKWOas0XSxt881bz04seizkoanA32iftkc130_assertion wasDerivedFrom ctd_human-20130708 NP20761.RAaVF8iALZUIKWOas0XSxt881bz04seizkoanA32iftkc130_provenance.
- NP20761.RAaVF8iALZUIKWOas0XSxt881bz04seizkoanA32iftkc130_assertion wasGeneratedBy ECO_0000218 NP20761.RAaVF8iALZUIKWOas0XSxt881bz04seizkoanA32iftkc130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP20761.RAaVF8iALZUIKWOas0XSxt881bz04seizkoanA32iftkc130_provenance.