Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP679395.RAbuKngnTBLkGaRJJvjrm4rx4BsHLW2Gsg8XMtxZWrELM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP679395.RAbuKngnTBLkGaRJJvjrm4rx4BsHLW2Gsg8XMtxZWrELM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP679395.RAbuKngnTBLkGaRJJvjrm4rx4BsHLW2Gsg8XMtxZWrELM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP679395.RAbuKngnTBLkGaRJJvjrm4rx4BsHLW2Gsg8XMtxZWrELM130_provenance.
- NP679395.RAbuKngnTBLkGaRJJvjrm4rx4BsHLW2Gsg8XMtxZWrELM130_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." NP679395.RAbuKngnTBLkGaRJJvjrm4rx4BsHLW2Gsg8XMtxZWrELM130_provenance.
- NP679395.RAbuKngnTBLkGaRJJvjrm4rx4BsHLW2Gsg8XMtxZWrELM130_assertion evidence source_evidence_literature NP679395.RAbuKngnTBLkGaRJJvjrm4rx4BsHLW2Gsg8XMtxZWrELM130_provenance.
- NP679395.RAbuKngnTBLkGaRJJvjrm4rx4BsHLW2Gsg8XMtxZWrELM130_assertion SIO_000772 10493832 NP679395.RAbuKngnTBLkGaRJJvjrm4rx4BsHLW2Gsg8XMtxZWrELM130_provenance.
- NP679395.RAbuKngnTBLkGaRJJvjrm4rx4BsHLW2Gsg8XMtxZWrELM130_assertion wasDerivedFrom befree-20140225 NP679395.RAbuKngnTBLkGaRJJvjrm4rx4BsHLW2Gsg8XMtxZWrELM130_provenance.
- NP679395.RAbuKngnTBLkGaRJJvjrm4rx4BsHLW2Gsg8XMtxZWrELM130_assertion wasGeneratedBy ECO_0000203 NP679395.RAbuKngnTBLkGaRJJvjrm4rx4BsHLW2Gsg8XMtxZWrELM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP679395.RAbuKngnTBLkGaRJJvjrm4rx4BsHLW2Gsg8XMtxZWrELM130_provenance.