Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP518232.RALUCgLy0bP4Jlsh0SzgcksMtegXdb7YlT9wrwy3YRy8U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP518232.RALUCgLy0bP4Jlsh0SzgcksMtegXdb7YlT9wrwy3YRy8U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP518232.RALUCgLy0bP4Jlsh0SzgcksMtegXdb7YlT9wrwy3YRy8U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP518232.RALUCgLy0bP4Jlsh0SzgcksMtegXdb7YlT9wrwy3YRy8U130_provenance.
- NP518232.RALUCgLy0bP4Jlsh0SzgcksMtegXdb7YlT9wrwy3YRy8U130_assertion description "[Taken together with previous findings of GRIA3 disruptions in the patients with MR, our study strengthens the idea that GRIA3 is a candidate gene for X-linked MR and that severely reduced GRIA3 expression results in MR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518232.RALUCgLy0bP4Jlsh0SzgcksMtegXdb7YlT9wrwy3YRy8U130_provenance.
- NP518232.RALUCgLy0bP4Jlsh0SzgcksMtegXdb7YlT9wrwy3YRy8U130_assertion evidence source_evidence_literature NP518232.RALUCgLy0bP4Jlsh0SzgcksMtegXdb7YlT9wrwy3YRy8U130_provenance.
- NP518232.RALUCgLy0bP4Jlsh0SzgcksMtegXdb7YlT9wrwy3YRy8U130_assertion SIO_000772 17568425 NP518232.RALUCgLy0bP4Jlsh0SzgcksMtegXdb7YlT9wrwy3YRy8U130_provenance.
- NP518232.RALUCgLy0bP4Jlsh0SzgcksMtegXdb7YlT9wrwy3YRy8U130_assertion wasDerivedFrom befree-20140225 NP518232.RALUCgLy0bP4Jlsh0SzgcksMtegXdb7YlT9wrwy3YRy8U130_provenance.
- NP518232.RALUCgLy0bP4Jlsh0SzgcksMtegXdb7YlT9wrwy3YRy8U130_assertion wasGeneratedBy ECO_0000203 NP518232.RALUCgLy0bP4Jlsh0SzgcksMtegXdb7YlT9wrwy3YRy8U130_provenance.
- befree-20140225 importedOn "2014-02-25" NP518232.RALUCgLy0bP4Jlsh0SzgcksMtegXdb7YlT9wrwy3YRy8U130_provenance.