Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP608266.RAqBvuSGNaozpnPCr5cB7aJbTt_M_bnY_U_lhdE1ZCexs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP608266.RAqBvuSGNaozpnPCr5cB7aJbTt_M_bnY_U_lhdE1ZCexs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP608266.RAqBvuSGNaozpnPCr5cB7aJbTt_M_bnY_U_lhdE1ZCexs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP608266.RAqBvuSGNaozpnPCr5cB7aJbTt_M_bnY_U_lhdE1ZCexs130_provenance.
- NP608266.RAqBvuSGNaozpnPCr5cB7aJbTt_M_bnY_U_lhdE1ZCexs130_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." NP608266.RAqBvuSGNaozpnPCr5cB7aJbTt_M_bnY_U_lhdE1ZCexs130_provenance.
- NP608266.RAqBvuSGNaozpnPCr5cB7aJbTt_M_bnY_U_lhdE1ZCexs130_assertion evidence source_evidence_literature NP608266.RAqBvuSGNaozpnPCr5cB7aJbTt_M_bnY_U_lhdE1ZCexs130_provenance.
- NP608266.RAqBvuSGNaozpnPCr5cB7aJbTt_M_bnY_U_lhdE1ZCexs130_assertion SIO_000772 10493832 NP608266.RAqBvuSGNaozpnPCr5cB7aJbTt_M_bnY_U_lhdE1ZCexs130_provenance.
- NP608266.RAqBvuSGNaozpnPCr5cB7aJbTt_M_bnY_U_lhdE1ZCexs130_assertion wasDerivedFrom befree-20150227 NP608266.RAqBvuSGNaozpnPCr5cB7aJbTt_M_bnY_U_lhdE1ZCexs130_provenance.
- NP608266.RAqBvuSGNaozpnPCr5cB7aJbTt_M_bnY_U_lhdE1ZCexs130_assertion wasGeneratedBy ECO_0000203 NP608266.RAqBvuSGNaozpnPCr5cB7aJbTt_M_bnY_U_lhdE1ZCexs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP608266.RAqBvuSGNaozpnPCr5cB7aJbTt_M_bnY_U_lhdE1ZCexs130_provenance.