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- source_evidence_literature type ECO_0000212 NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_provenance.
- NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_assertion description "[Two families with a retinal dystrophy were extensively phenotyped and blood was taken for mutation analysis of the RDS (all) and ROM1 (retinitis pigmentosa patients only) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_provenance.
- NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_assertion evidence source_evidence_literature NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_provenance.
- NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_assertion SIO_000772 16916875 NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_provenance.
- NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_assertion wasDerivedFrom befree-20150227 NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_provenance.
- NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_assertion wasGeneratedBy ECO_0000203 NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP674105.RAryehclnKfj6JavngxXWbME-ZXuHBNbq6rq6uq1LHZ-s130_provenance.