Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP499606.RAbCPy1Y6JaB4knfHPBSuFCQxG3zVlKlIXW5Z-Epoo5Lg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP499606.RAbCPy1Y6JaB4knfHPBSuFCQxG3zVlKlIXW5Z-Epoo5Lg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499606.RAbCPy1Y6JaB4knfHPBSuFCQxG3zVlKlIXW5Z-Epoo5Lg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499606.RAbCPy1Y6JaB4knfHPBSuFCQxG3zVlKlIXW5Z-Epoo5Lg130_provenance.
- NP499606.RAbCPy1Y6JaB4knfHPBSuFCQxG3zVlKlIXW5Z-Epoo5Lg130_assertion description "[A locus (LCA3) for Leber congenital amaurosis, a severe, early-onset form of arRD, maps close to RDH12 on chromosome 14q24.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499606.RAbCPy1Y6JaB4knfHPBSuFCQxG3zVlKlIXW5Z-Epoo5Lg130_provenance.
- NP499606.RAbCPy1Y6JaB4knfHPBSuFCQxG3zVlKlIXW5Z-Epoo5Lg130_assertion evidence source_evidence_literature NP499606.RAbCPy1Y6JaB4knfHPBSuFCQxG3zVlKlIXW5Z-Epoo5Lg130_provenance.
- NP499606.RAbCPy1Y6JaB4knfHPBSuFCQxG3zVlKlIXW5Z-Epoo5Lg130_assertion SIO_000772 16269441 NP499606.RAbCPy1Y6JaB4knfHPBSuFCQxG3zVlKlIXW5Z-Epoo5Lg130_provenance.
- NP499606.RAbCPy1Y6JaB4knfHPBSuFCQxG3zVlKlIXW5Z-Epoo5Lg130_assertion wasDerivedFrom befree-20140225 NP499606.RAbCPy1Y6JaB4knfHPBSuFCQxG3zVlKlIXW5Z-Epoo5Lg130_provenance.
- NP499606.RAbCPy1Y6JaB4knfHPBSuFCQxG3zVlKlIXW5Z-Epoo5Lg130_assertion wasGeneratedBy ECO_0000203 NP499606.RAbCPy1Y6JaB4knfHPBSuFCQxG3zVlKlIXW5Z-Epoo5Lg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP499606.RAbCPy1Y6JaB4knfHPBSuFCQxG3zVlKlIXW5Z-Epoo5Lg130_provenance.