Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP451617.RAvq1DVUxkG17cDsefpO_7cyLQdVy3tSdSJI5_VX8PY4Y130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP451617.RAvq1DVUxkG17cDsefpO_7cyLQdVy3tSdSJI5_VX8PY4Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP451617.RAvq1DVUxkG17cDsefpO_7cyLQdVy3tSdSJI5_VX8PY4Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP451617.RAvq1DVUxkG17cDsefpO_7cyLQdVy3tSdSJI5_VX8PY4Y130_provenance.
- NP451617.RAvq1DVUxkG17cDsefpO_7cyLQdVy3tSdSJI5_VX8PY4Y130_assertion description "[Mutations in the Aristaless-related homeobox (ARX) gene are associated with a broad spectrum of disorders including X-linked lissencephaly with abnormal genitalia (XLAG) and absent corpus callosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP451617.RAvq1DVUxkG17cDsefpO_7cyLQdVy3tSdSJI5_VX8PY4Y130_provenance.
- NP451617.RAvq1DVUxkG17cDsefpO_7cyLQdVy3tSdSJI5_VX8PY4Y130_assertion evidence source_evidence_literature NP451617.RAvq1DVUxkG17cDsefpO_7cyLQdVy3tSdSJI5_VX8PY4Y130_provenance.
- NP451617.RAvq1DVUxkG17cDsefpO_7cyLQdVy3tSdSJI5_VX8PY4Y130_assertion SIO_000772 15248097 NP451617.RAvq1DVUxkG17cDsefpO_7cyLQdVy3tSdSJI5_VX8PY4Y130_provenance.
- NP451617.RAvq1DVUxkG17cDsefpO_7cyLQdVy3tSdSJI5_VX8PY4Y130_assertion wasDerivedFrom befree-2016 NP451617.RAvq1DVUxkG17cDsefpO_7cyLQdVy3tSdSJI5_VX8PY4Y130_provenance.
- NP451617.RAvq1DVUxkG17cDsefpO_7cyLQdVy3tSdSJI5_VX8PY4Y130_assertion wasGeneratedBy ECO_0000203 NP451617.RAvq1DVUxkG17cDsefpO_7cyLQdVy3tSdSJI5_VX8PY4Y130_provenance.
- befree-2016 importedOn "2016-02-19" NP451617.RAvq1DVUxkG17cDsefpO_7cyLQdVy3tSdSJI5_VX8PY4Y130_provenance.