Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_provenance.
- NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_assertion description "[Mutations in the human transmembrane protein CRB1 are associated with severe forms of retinal dystrophy, retinitis pigmentosa 12 (RP12), and Leber's congenital amaurosis (LCA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_provenance.
- NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_assertion evidence source_evidence_literature NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_provenance.
- NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_assertion SIO_000772 12361571 NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_provenance.
- NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_assertion wasDerivedFrom befree-20140225 NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_provenance.
- NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_assertion wasGeneratedBy ECO_0000203 NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP588525.RACPYMjMINvsYen0ZmhJ7acPKf40_XxOz1_CKrdk4MGUs130_provenance.