Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP601314.RAb40Ptm1dTRBwb8ZKMZgJs3ZnQz9S-1TpFTo_A5w_Y2Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP601314.RAb40Ptm1dTRBwb8ZKMZgJs3ZnQz9S-1TpFTo_A5w_Y2Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP601314.RAb40Ptm1dTRBwb8ZKMZgJs3ZnQz9S-1TpFTo_A5w_Y2Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP601314.RAb40Ptm1dTRBwb8ZKMZgJs3ZnQz9S-1TpFTo_A5w_Y2Q130_provenance.
- NP601314.RAb40Ptm1dTRBwb8ZKMZgJs3ZnQz9S-1TpFTo_A5w_Y2Q130_assertion description "[Ten mutations in the guanylate cyclase activator 1A (GUCA1A) have been previously identified and reported in patients with retinal degeneration, including patients from 12 families with cone-rod dystrophy (CORD) and in an isolated patient with retinitis pigmentosa (RP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP601314.RAb40Ptm1dTRBwb8ZKMZgJs3ZnQz9S-1TpFTo_A5w_Y2Q130_provenance.
- NP601314.RAb40Ptm1dTRBwb8ZKMZgJs3ZnQz9S-1TpFTo_A5w_Y2Q130_assertion evidence source_evidence_literature NP601314.RAb40Ptm1dTRBwb8ZKMZgJs3ZnQz9S-1TpFTo_A5w_Y2Q130_provenance.
- NP601314.RAb40Ptm1dTRBwb8ZKMZgJs3ZnQz9S-1TpFTo_A5w_Y2Q130_assertion SIO_000772 23428504 NP601314.RAb40Ptm1dTRBwb8ZKMZgJs3ZnQz9S-1TpFTo_A5w_Y2Q130_provenance.
- NP601314.RAb40Ptm1dTRBwb8ZKMZgJs3ZnQz9S-1TpFTo_A5w_Y2Q130_assertion wasDerivedFrom befree-20140225 NP601314.RAb40Ptm1dTRBwb8ZKMZgJs3ZnQz9S-1TpFTo_A5w_Y2Q130_provenance.
- NP601314.RAb40Ptm1dTRBwb8ZKMZgJs3ZnQz9S-1TpFTo_A5w_Y2Q130_assertion wasGeneratedBy ECO_0000203 NP601314.RAb40Ptm1dTRBwb8ZKMZgJs3ZnQz9S-1TpFTo_A5w_Y2Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP601314.RAb40Ptm1dTRBwb8ZKMZgJs3ZnQz9S-1TpFTo_A5w_Y2Q130_provenance.