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- source_evidence_literature type ECO_0000212 NP569567.RA8pNWl_xn16pe3QIpSBrKp7gzHUTnSiiRY1NMkfsWWFg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569567.RA8pNWl_xn16pe3QIpSBrKp7gzHUTnSiiRY1NMkfsWWFg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569567.RA8pNWl_xn16pe3QIpSBrKp7gzHUTnSiiRY1NMkfsWWFg130_provenance.
- NP569567.RA8pNWl_xn16pe3QIpSBrKp7gzHUTnSiiRY1NMkfsWWFg130_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." NP569567.RA8pNWl_xn16pe3QIpSBrKp7gzHUTnSiiRY1NMkfsWWFg130_provenance.
- NP569567.RA8pNWl_xn16pe3QIpSBrKp7gzHUTnSiiRY1NMkfsWWFg130_assertion evidence source_evidence_literature NP569567.RA8pNWl_xn16pe3QIpSBrKp7gzHUTnSiiRY1NMkfsWWFg130_provenance.
- NP569567.RA8pNWl_xn16pe3QIpSBrKp7gzHUTnSiiRY1NMkfsWWFg130_assertion SIO_000772 10493832 NP569567.RA8pNWl_xn16pe3QIpSBrKp7gzHUTnSiiRY1NMkfsWWFg130_provenance.
- NP569567.RA8pNWl_xn16pe3QIpSBrKp7gzHUTnSiiRY1NMkfsWWFg130_assertion wasDerivedFrom befree-20150227 NP569567.RA8pNWl_xn16pe3QIpSBrKp7gzHUTnSiiRY1NMkfsWWFg130_provenance.
- NP569567.RA8pNWl_xn16pe3QIpSBrKp7gzHUTnSiiRY1NMkfsWWFg130_assertion wasGeneratedBy ECO_0000203 NP569567.RA8pNWl_xn16pe3QIpSBrKp7gzHUTnSiiRY1NMkfsWWFg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP569567.RA8pNWl_xn16pe3QIpSBrKp7gzHUTnSiiRY1NMkfsWWFg130_provenance.