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- source_evidence_literature type ECO_0000212 NP67981.RA66Lzv0Vwks0V-9Ei8XWh3JjXvMjqQ9X_uXh7J37mza0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP67981.RA66Lzv0Vwks0V-9Ei8XWh3JjXvMjqQ9X_uXh7J37mza0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP67981.RA66Lzv0Vwks0V-9Ei8XWh3JjXvMjqQ9X_uXh7J37mza0130_provenance.
- NP67981.RA66Lzv0Vwks0V-9Ei8XWh3JjXvMjqQ9X_uXh7J37mza0130_assertion description "[In a Portuguese population of 45 HCM patients, 5 (11.1%) had mutations in the MYBPC3 gene (3 missense mutations--theoretically less frequent in the MYBPC3 gene--and 2 deletions).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP67981.RA66Lzv0Vwks0V-9Ei8XWh3JjXvMjqQ9X_uXh7J37mza0130_provenance.
- NP67981.RA66Lzv0Vwks0V-9Ei8XWh3JjXvMjqQ9X_uXh7J37mza0130_assertion evidence source_evidence_literature NP67981.RA66Lzv0Vwks0V-9Ei8XWh3JjXvMjqQ9X_uXh7J37mza0130_provenance.
- NP67981.RA66Lzv0Vwks0V-9Ei8XWh3JjXvMjqQ9X_uXh7J37mza0130_assertion SIO_000772 16566405 NP67981.RA66Lzv0Vwks0V-9Ei8XWh3JjXvMjqQ9X_uXh7J37mza0130_provenance.
- NP67981.RA66Lzv0Vwks0V-9Ei8XWh3JjXvMjqQ9X_uXh7J37mza0130_assertion wasDerivedFrom gad-20150221 NP67981.RA66Lzv0Vwks0V-9Ei8XWh3JjXvMjqQ9X_uXh7J37mza0130_provenance.
- NP67981.RA66Lzv0Vwks0V-9Ei8XWh3JjXvMjqQ9X_uXh7J37mza0130_assertion wasGeneratedBy ECO_0000203 NP67981.RA66Lzv0Vwks0V-9Ei8XWh3JjXvMjqQ9X_uXh7J37mza0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP67981.RA66Lzv0Vwks0V-9Ei8XWh3JjXvMjqQ9X_uXh7J37mza0130_provenance.