Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP762179.RAdnwu-nQzDk8kOWIiR_GH7jIlw0ZvfFuxdiuaNKcr2mY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP762179.RAdnwu-nQzDk8kOWIiR_GH7jIlw0ZvfFuxdiuaNKcr2mY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP762179.RAdnwu-nQzDk8kOWIiR_GH7jIlw0ZvfFuxdiuaNKcr2mY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP762179.RAdnwu-nQzDk8kOWIiR_GH7jIlw0ZvfFuxdiuaNKcr2mY130_provenance.
- NP762179.RAdnwu-nQzDk8kOWIiR_GH7jIlw0ZvfFuxdiuaNKcr2mY130_assertion description "[Ohtahara syndrome in a family with an ARX protein truncation mutation (c.81C>G/p.Y27X).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762179.RAdnwu-nQzDk8kOWIiR_GH7jIlw0ZvfFuxdiuaNKcr2mY130_provenance.
- NP762179.RAdnwu-nQzDk8kOWIiR_GH7jIlw0ZvfFuxdiuaNKcr2mY130_assertion evidence source_evidence_literature NP762179.RAdnwu-nQzDk8kOWIiR_GH7jIlw0ZvfFuxdiuaNKcr2mY130_provenance.
- NP762179.RAdnwu-nQzDk8kOWIiR_GH7jIlw0ZvfFuxdiuaNKcr2mY130_assertion SIO_000772 19738637 NP762179.RAdnwu-nQzDk8kOWIiR_GH7jIlw0ZvfFuxdiuaNKcr2mY130_provenance.
- NP762179.RAdnwu-nQzDk8kOWIiR_GH7jIlw0ZvfFuxdiuaNKcr2mY130_assertion wasDerivedFrom befree-2016 NP762179.RAdnwu-nQzDk8kOWIiR_GH7jIlw0ZvfFuxdiuaNKcr2mY130_provenance.
- NP762179.RAdnwu-nQzDk8kOWIiR_GH7jIlw0ZvfFuxdiuaNKcr2mY130_assertion wasGeneratedBy ECO_0000203 NP762179.RAdnwu-nQzDk8kOWIiR_GH7jIlw0ZvfFuxdiuaNKcr2mY130_provenance.
- befree-2016 importedOn "2016-02-19" NP762179.RAdnwu-nQzDk8kOWIiR_GH7jIlw0ZvfFuxdiuaNKcr2mY130_provenance.