Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP898121.RAg3dfOtRc0qCxGVrsdL6XRHiEaSheVxPREDBOF5IO91E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP898121.RAg3dfOtRc0qCxGVrsdL6XRHiEaSheVxPREDBOF5IO91E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP898121.RAg3dfOtRc0qCxGVrsdL6XRHiEaSheVxPREDBOF5IO91E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP898121.RAg3dfOtRc0qCxGVrsdL6XRHiEaSheVxPREDBOF5IO91E130_provenance.
- NP898121.RAg3dfOtRc0qCxGVrsdL6XRHiEaSheVxPREDBOF5IO91E130_assertion description "[The other two presented similar clinical manifestations of dRTA and different mutations in the ATP6V0A4 gene: one patient, showing EVA, developed an early SNHL, whereas in the other one, the SNHL appeared in the second decade of life and the vestibular aqueduct was normal.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898121.RAg3dfOtRc0qCxGVrsdL6XRHiEaSheVxPREDBOF5IO91E130_provenance.
- NP898121.RAg3dfOtRc0qCxGVrsdL6XRHiEaSheVxPREDBOF5IO91E130_assertion evidence source_evidence_literature NP898121.RAg3dfOtRc0qCxGVrsdL6XRHiEaSheVxPREDBOF5IO91E130_provenance.
- NP898121.RAg3dfOtRc0qCxGVrsdL6XRHiEaSheVxPREDBOF5IO91E130_assertion SIO_000772 19639346 NP898121.RAg3dfOtRc0qCxGVrsdL6XRHiEaSheVxPREDBOF5IO91E130_provenance.
- NP898121.RAg3dfOtRc0qCxGVrsdL6XRHiEaSheVxPREDBOF5IO91E130_assertion wasDerivedFrom befree-20150227 NP898121.RAg3dfOtRc0qCxGVrsdL6XRHiEaSheVxPREDBOF5IO91E130_provenance.
- NP898121.RAg3dfOtRc0qCxGVrsdL6XRHiEaSheVxPREDBOF5IO91E130_assertion wasGeneratedBy ECO_0000203 NP898121.RAg3dfOtRc0qCxGVrsdL6XRHiEaSheVxPREDBOF5IO91E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP898121.RAg3dfOtRc0qCxGVrsdL6XRHiEaSheVxPREDBOF5IO91E130_provenance.