Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP350668.RAgASL_MA9hVsS0n6kGS92IZydFgH0qYxS5eR_WsQY_vc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP350668.RAgASL_MA9hVsS0n6kGS92IZydFgH0qYxS5eR_WsQY_vc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP350668.RAgASL_MA9hVsS0n6kGS92IZydFgH0qYxS5eR_WsQY_vc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP350668.RAgASL_MA9hVsS0n6kGS92IZydFgH0qYxS5eR_WsQY_vc130_provenance.
- NP350668.RAgASL_MA9hVsS0n6kGS92IZydFgH0qYxS5eR_WsQY_vc130_assertion description "[A novel human gene, TRPC5, was cloned from the region of Xq23 that contains loci for nonsyndromic mental retardation (MRX47 and MRX35) and two genes, DCX and HPAK3, implicated in two X-linked disorders (LISX and MRX30).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP350668.RAgASL_MA9hVsS0n6kGS92IZydFgH0qYxS5eR_WsQY_vc130_provenance.
- NP350668.RAgASL_MA9hVsS0n6kGS92IZydFgH0qYxS5eR_WsQY_vc130_assertion evidence source_evidence_literature NP350668.RAgASL_MA9hVsS0n6kGS92IZydFgH0qYxS5eR_WsQY_vc130_provenance.
- NP350668.RAgASL_MA9hVsS0n6kGS92IZydFgH0qYxS5eR_WsQY_vc130_assertion SIO_000772 10493832 NP350668.RAgASL_MA9hVsS0n6kGS92IZydFgH0qYxS5eR_WsQY_vc130_provenance.
- NP350668.RAgASL_MA9hVsS0n6kGS92IZydFgH0qYxS5eR_WsQY_vc130_assertion wasDerivedFrom befree-20150227 NP350668.RAgASL_MA9hVsS0n6kGS92IZydFgH0qYxS5eR_WsQY_vc130_provenance.
- NP350668.RAgASL_MA9hVsS0n6kGS92IZydFgH0qYxS5eR_WsQY_vc130_assertion wasGeneratedBy ECO_0000203 NP350668.RAgASL_MA9hVsS0n6kGS92IZydFgH0qYxS5eR_WsQY_vc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP350668.RAgASL_MA9hVsS0n6kGS92IZydFgH0qYxS5eR_WsQY_vc130_provenance.