Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_provenance.
- NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_assertion description "[Aristaless-related homeobox gene (ARX) mutation leads to several neurological disorders including X-linked lissencephaly with abnormal genitalia (XLAG), West syndrome and Partington syndrome, with XLAG being the most severe form.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_provenance.
- NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_assertion evidence source_evidence_literature NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_provenance.
- NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_assertion SIO_000772 20538404 NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_provenance.
- NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_assertion wasDerivedFrom befree-2016 NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_provenance.
- NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_assertion wasGeneratedBy ECO_0000203 NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_provenance.
- befree-2016 importedOn "2016-02-19" NP817894.RABD1HpmQmJTl22q_imIxUhbwk6GN6dqdgg-0i7jJxdWY130_provenance.