Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_provenance.
- NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_assertion description "[Mutations in SLC6A5, encoding GlyT2, cause hereditary hyperekplexia in humans, and similar phenotypes in knock-out mice, and variants are associated with schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_provenance.
- NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_assertion evidence source_evidence_literature NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_provenance.
- NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_assertion SIO_000772 22272310 NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_provenance.
- NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_assertion wasDerivedFrom befree-20140225 NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_provenance.
- NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_assertion wasGeneratedBy ECO_0000203 NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP598976.RAVURfiXy2T3iJFMmamQqZctkY46svizDI6jhr45HZYx0130_provenance.