Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP785794.RAlLMnXMVdx8yPhuUGgYJDSUJM5A-DrgnCgOz8iEayfp0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP785794.RAlLMnXMVdx8yPhuUGgYJDSUJM5A-DrgnCgOz8iEayfp0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP785794.RAlLMnXMVdx8yPhuUGgYJDSUJM5A-DrgnCgOz8iEayfp0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP785794.RAlLMnXMVdx8yPhuUGgYJDSUJM5A-DrgnCgOz8iEayfp0130_provenance.
- NP785794.RAlLMnXMVdx8yPhuUGgYJDSUJM5A-DrgnCgOz8iEayfp0130_assertion description "[Mutations in the Usher syndrome type I causing genes are also recorded in non-syndromic hearing loss cases and mutations in USH2A in non-syndromic retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP785794.RAlLMnXMVdx8yPhuUGgYJDSUJM5A-DrgnCgOz8iEayfp0130_provenance.
- NP785794.RAlLMnXMVdx8yPhuUGgYJDSUJM5A-DrgnCgOz8iEayfp0130_assertion evidence source_evidence_literature NP785794.RAlLMnXMVdx8yPhuUGgYJDSUJM5A-DrgnCgOz8iEayfp0130_provenance.
- NP785794.RAlLMnXMVdx8yPhuUGgYJDSUJM5A-DrgnCgOz8iEayfp0130_assertion SIO_000772 18484607 NP785794.RAlLMnXMVdx8yPhuUGgYJDSUJM5A-DrgnCgOz8iEayfp0130_provenance.
- NP785794.RAlLMnXMVdx8yPhuUGgYJDSUJM5A-DrgnCgOz8iEayfp0130_assertion wasDerivedFrom befree-20140225 NP785794.RAlLMnXMVdx8yPhuUGgYJDSUJM5A-DrgnCgOz8iEayfp0130_provenance.
- NP785794.RAlLMnXMVdx8yPhuUGgYJDSUJM5A-DrgnCgOz8iEayfp0130_assertion wasGeneratedBy ECO_0000203 NP785794.RAlLMnXMVdx8yPhuUGgYJDSUJM5A-DrgnCgOz8iEayfp0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP785794.RAlLMnXMVdx8yPhuUGgYJDSUJM5A-DrgnCgOz8iEayfp0130_provenance.