Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP720864.RAKYGzZxO4HhoJ_yvPiyMHPuA75ay4N5v6LhEWIBaJQKs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP720864.RAKYGzZxO4HhoJ_yvPiyMHPuA75ay4N5v6LhEWIBaJQKs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP720864.RAKYGzZxO4HhoJ_yvPiyMHPuA75ay4N5v6LhEWIBaJQKs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP720864.RAKYGzZxO4HhoJ_yvPiyMHPuA75ay4N5v6LhEWIBaJQKs130_provenance.
- NP720864.RAKYGzZxO4HhoJ_yvPiyMHPuA75ay4N5v6LhEWIBaJQKs130_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." NP720864.RAKYGzZxO4HhoJ_yvPiyMHPuA75ay4N5v6LhEWIBaJQKs130_provenance.
- NP720864.RAKYGzZxO4HhoJ_yvPiyMHPuA75ay4N5v6LhEWIBaJQKs130_assertion evidence source_evidence_literature NP720864.RAKYGzZxO4HhoJ_yvPiyMHPuA75ay4N5v6LhEWIBaJQKs130_provenance.
- NP720864.RAKYGzZxO4HhoJ_yvPiyMHPuA75ay4N5v6LhEWIBaJQKs130_assertion SIO_000772 20538404 NP720864.RAKYGzZxO4HhoJ_yvPiyMHPuA75ay4N5v6LhEWIBaJQKs130_provenance.
- NP720864.RAKYGzZxO4HhoJ_yvPiyMHPuA75ay4N5v6LhEWIBaJQKs130_assertion wasDerivedFrom befree-20140225 NP720864.RAKYGzZxO4HhoJ_yvPiyMHPuA75ay4N5v6LhEWIBaJQKs130_provenance.
- NP720864.RAKYGzZxO4HhoJ_yvPiyMHPuA75ay4N5v6LhEWIBaJQKs130_assertion wasGeneratedBy ECO_0000203 NP720864.RAKYGzZxO4HhoJ_yvPiyMHPuA75ay4N5v6LhEWIBaJQKs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP720864.RAKYGzZxO4HhoJ_yvPiyMHPuA75ay4N5v6LhEWIBaJQKs130_provenance.