Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP183986.RAWHPXSyOqMuluGWUNaysJHNvVVEOD2nvRHH5Hvllw1yc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP183986.RAWHPXSyOqMuluGWUNaysJHNvVVEOD2nvRHH5Hvllw1yc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP183986.RAWHPXSyOqMuluGWUNaysJHNvVVEOD2nvRHH5Hvllw1yc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP183986.RAWHPXSyOqMuluGWUNaysJHNvVVEOD2nvRHH5Hvllw1yc130_provenance.
- NP183986.RAWHPXSyOqMuluGWUNaysJHNvVVEOD2nvRHH5Hvllw1yc130_assertion description "[This is the third reported mutation in CERKL causing retinal degeneration but is the first report to show that a single amino acid change in CERKL, rather than a null mutation, can cause retinal disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP183986.RAWHPXSyOqMuluGWUNaysJHNvVVEOD2nvRHH5Hvllw1yc130_provenance.
- NP183986.RAWHPXSyOqMuluGWUNaysJHNvVVEOD2nvRHH5Hvllw1yc130_assertion evidence source_evidence_literature NP183986.RAWHPXSyOqMuluGWUNaysJHNvVVEOD2nvRHH5Hvllw1yc130_provenance.
- NP183986.RAWHPXSyOqMuluGWUNaysJHNvVVEOD2nvRHH5Hvllw1yc130_assertion SIO_000772 18978954 NP183986.RAWHPXSyOqMuluGWUNaysJHNvVVEOD2nvRHH5Hvllw1yc130_provenance.
- NP183986.RAWHPXSyOqMuluGWUNaysJHNvVVEOD2nvRHH5Hvllw1yc130_assertion wasDerivedFrom lhgdn-20090331 NP183986.RAWHPXSyOqMuluGWUNaysJHNvVVEOD2nvRHH5Hvllw1yc130_provenance.
- NP183986.RAWHPXSyOqMuluGWUNaysJHNvVVEOD2nvRHH5Hvllw1yc130_assertion wasGeneratedBy ECO_0000203 NP183986.RAWHPXSyOqMuluGWUNaysJHNvVVEOD2nvRHH5Hvllw1yc130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP183986.RAWHPXSyOqMuluGWUNaysJHNvVVEOD2nvRHH5Hvllw1yc130_provenance.