Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_provenance.
- NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_assertion description "[The molecular genetic analysis demonstrated the APTX mutation W279X at locus 9p13.3 (ataxia with oculomotor apraxia 1 disease), and psychologic studies showed mild cognitive impairment.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_provenance.
- NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_assertion evidence source_evidence_literature NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_provenance.
- NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_assertion SIO_000772 15996403 NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_provenance.
- NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_assertion wasDerivedFrom befree-2016 NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_provenance.
- NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_assertion wasGeneratedBy ECO_0000203 NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_provenance.
- befree-2016 importedOn "2016-02-19" NP502346.RAAYfbJ1IZlakzXFpS-Rlqs25T3GXkxB-GUaKH7yex9eo130_provenance.