Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP569899.RAhMu9BInRh6_w4xoGjb7qqqtLEq1ATGgVbqxeCIMM47I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP569899.RAhMu9BInRh6_w4xoGjb7qqqtLEq1ATGgVbqxeCIMM47I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569899.RAhMu9BInRh6_w4xoGjb7qqqtLEq1ATGgVbqxeCIMM47I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569899.RAhMu9BInRh6_w4xoGjb7qqqtLEq1ATGgVbqxeCIMM47I130_provenance.
- NP569899.RAhMu9BInRh6_w4xoGjb7qqqtLEq1ATGgVbqxeCIMM47I130_assertion description "[Mutations in RLBP1 were identified in 7 patients with RPA and in 1 patient with FAP and cone dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569899.RAhMu9BInRh6_w4xoGjb7qqqtLEq1ATGgVbqxeCIMM47I130_provenance.
- NP569899.RAhMu9BInRh6_w4xoGjb7qqqtLEq1ATGgVbqxeCIMM47I130_assertion evidence source_evidence_literature NP569899.RAhMu9BInRh6_w4xoGjb7qqqtLEq1ATGgVbqxeCIMM47I130_provenance.
- NP569899.RAhMu9BInRh6_w4xoGjb7qqqtLEq1ATGgVbqxeCIMM47I130_assertion SIO_000772 22559933 NP569899.RAhMu9BInRh6_w4xoGjb7qqqtLEq1ATGgVbqxeCIMM47I130_provenance.
- NP569899.RAhMu9BInRh6_w4xoGjb7qqqtLEq1ATGgVbqxeCIMM47I130_assertion wasDerivedFrom befree-20140225 NP569899.RAhMu9BInRh6_w4xoGjb7qqqtLEq1ATGgVbqxeCIMM47I130_provenance.
- NP569899.RAhMu9BInRh6_w4xoGjb7qqqtLEq1ATGgVbqxeCIMM47I130_assertion wasGeneratedBy ECO_0000203 NP569899.RAhMu9BInRh6_w4xoGjb7qqqtLEq1ATGgVbqxeCIMM47I130_provenance.
- befree-20140225 importedOn "2014-02-25" NP569899.RAhMu9BInRh6_w4xoGjb7qqqtLEq1ATGgVbqxeCIMM47I130_provenance.