Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP905614.RAk192ubYJGjpsUWQF5kXNPnKoX5Hio_5gB1KhrXV1NzY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP905614.RAk192ubYJGjpsUWQF5kXNPnKoX5Hio_5gB1KhrXV1NzY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP905614.RAk192ubYJGjpsUWQF5kXNPnKoX5Hio_5gB1KhrXV1NzY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP905614.RAk192ubYJGjpsUWQF5kXNPnKoX5Hio_5gB1KhrXV1NzY130_provenance.
- NP905614.RAk192ubYJGjpsUWQF5kXNPnKoX5Hio_5gB1KhrXV1NzY130_assertion description "[High incidence of right ventricular hypertrophy and left ventricular outflow tract obstruction are other prominent features of this novel PRKAG2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP905614.RAk192ubYJGjpsUWQF5kXNPnKoX5Hio_5gB1KhrXV1NzY130_provenance.
- NP905614.RAk192ubYJGjpsUWQF5kXNPnKoX5Hio_5gB1KhrXV1NzY130_assertion evidence source_evidence_literature NP905614.RAk192ubYJGjpsUWQF5kXNPnKoX5Hio_5gB1KhrXV1NzY130_provenance.
- NP905614.RAk192ubYJGjpsUWQF5kXNPnKoX5Hio_5gB1KhrXV1NzY130_assertion SIO_000772 16716659 NP905614.RAk192ubYJGjpsUWQF5kXNPnKoX5Hio_5gB1KhrXV1NzY130_provenance.
- NP905614.RAk192ubYJGjpsUWQF5kXNPnKoX5Hio_5gB1KhrXV1NzY130_assertion wasDerivedFrom befree-20150227 NP905614.RAk192ubYJGjpsUWQF5kXNPnKoX5Hio_5gB1KhrXV1NzY130_provenance.
- NP905614.RAk192ubYJGjpsUWQF5kXNPnKoX5Hio_5gB1KhrXV1NzY130_assertion wasGeneratedBy ECO_0000203 NP905614.RAk192ubYJGjpsUWQF5kXNPnKoX5Hio_5gB1KhrXV1NzY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP905614.RAk192ubYJGjpsUWQF5kXNPnKoX5Hio_5gB1KhrXV1NzY130_provenance.