Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP688848.RAuYDSzrpFf3ZjcETrSjAacJkW30W0YMl9FX-y8T27HHU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP688848.RAuYDSzrpFf3ZjcETrSjAacJkW30W0YMl9FX-y8T27HHU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP688848.RAuYDSzrpFf3ZjcETrSjAacJkW30W0YMl9FX-y8T27HHU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP688848.RAuYDSzrpFf3ZjcETrSjAacJkW30W0YMl9FX-y8T27HHU130_provenance.
- NP688848.RAuYDSzrpFf3ZjcETrSjAacJkW30W0YMl9FX-y8T27HHU130_assertion description "[One paraganglioma with no known SDH mutation but clinical features suggesting familial disease was negative, and one showed weak diffuse staining.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP688848.RAuYDSzrpFf3ZjcETrSjAacJkW30W0YMl9FX-y8T27HHU130_provenance.
- NP688848.RAuYDSzrpFf3ZjcETrSjAacJkW30W0YMl9FX-y8T27HHU130_assertion evidence source_evidence_literature NP688848.RAuYDSzrpFf3ZjcETrSjAacJkW30W0YMl9FX-y8T27HHU130_provenance.
- NP688848.RAuYDSzrpFf3ZjcETrSjAacJkW30W0YMl9FX-y8T27HHU130_assertion SIO_000772 20236688 NP688848.RAuYDSzrpFf3ZjcETrSjAacJkW30W0YMl9FX-y8T27HHU130_provenance.
- NP688848.RAuYDSzrpFf3ZjcETrSjAacJkW30W0YMl9FX-y8T27HHU130_assertion wasDerivedFrom befree-20150227 NP688848.RAuYDSzrpFf3ZjcETrSjAacJkW30W0YMl9FX-y8T27HHU130_provenance.
- NP688848.RAuYDSzrpFf3ZjcETrSjAacJkW30W0YMl9FX-y8T27HHU130_assertion wasGeneratedBy ECO_0000203 NP688848.RAuYDSzrpFf3ZjcETrSjAacJkW30W0YMl9FX-y8T27HHU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP688848.RAuYDSzrpFf3ZjcETrSjAacJkW30W0YMl9FX-y8T27HHU130_provenance.