Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP567497.RAt8k30LKRcHa4Mpn10WE3W0hi_g9WSA3C9fdOWKNDh5w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP567497.RAt8k30LKRcHa4Mpn10WE3W0hi_g9WSA3C9fdOWKNDh5w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP567497.RAt8k30LKRcHa4Mpn10WE3W0hi_g9WSA3C9fdOWKNDh5w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP567497.RAt8k30LKRcHa4Mpn10WE3W0hi_g9WSA3C9fdOWKNDh5w130_provenance.
- NP567497.RAt8k30LKRcHa4Mpn10WE3W0hi_g9WSA3C9fdOWKNDh5w130_assertion description "[Integrated YAC contig containing the 3p14.2 hereditary renal carcinoma 3;8 translocation breakpoint and the fragile site FRA3B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP567497.RAt8k30LKRcHa4Mpn10WE3W0hi_g9WSA3C9fdOWKNDh5w130_provenance.
- NP567497.RAt8k30LKRcHa4Mpn10WE3W0hi_g9WSA3C9fdOWKNDh5w130_assertion evidence source_evidence_literature NP567497.RAt8k30LKRcHa4Mpn10WE3W0hi_g9WSA3C9fdOWKNDh5w130_provenance.
- NP567497.RAt8k30LKRcHa4Mpn10WE3W0hi_g9WSA3C9fdOWKNDh5w130_assertion SIO_000772 7533524 NP567497.RAt8k30LKRcHa4Mpn10WE3W0hi_g9WSA3C9fdOWKNDh5w130_provenance.
- NP567497.RAt8k30LKRcHa4Mpn10WE3W0hi_g9WSA3C9fdOWKNDh5w130_assertion wasDerivedFrom befree-20140225 NP567497.RAt8k30LKRcHa4Mpn10WE3W0hi_g9WSA3C9fdOWKNDh5w130_provenance.
- NP567497.RAt8k30LKRcHa4Mpn10WE3W0hi_g9WSA3C9fdOWKNDh5w130_assertion wasGeneratedBy ECO_0000203 NP567497.RAt8k30LKRcHa4Mpn10WE3W0hi_g9WSA3C9fdOWKNDh5w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP567497.RAt8k30LKRcHa4Mpn10WE3W0hi_g9WSA3C9fdOWKNDh5w130_provenance.