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- source_evidence_literature type ECO_0000212 NP400621.RAnvInOkvhCNxrHItiu020lyH-dIc1FTT8d1zSxGbOztY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP400621.RAnvInOkvhCNxrHItiu020lyH-dIc1FTT8d1zSxGbOztY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP400621.RAnvInOkvhCNxrHItiu020lyH-dIc1FTT8d1zSxGbOztY130_provenance.
- NP400621.RAnvInOkvhCNxrHItiu020lyH-dIc1FTT8d1zSxGbOztY130_assertion description "[Recently, forms of syndromic and nonspecific X-linked mental retardation have been found to be associated with mutations in the Aristaless-related homeobox gene ARX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400621.RAnvInOkvhCNxrHItiu020lyH-dIc1FTT8d1zSxGbOztY130_provenance.
- NP400621.RAnvInOkvhCNxrHItiu020lyH-dIc1FTT8d1zSxGbOztY130_assertion evidence source_evidence_literature NP400621.RAnvInOkvhCNxrHItiu020lyH-dIc1FTT8d1zSxGbOztY130_provenance.
- NP400621.RAnvInOkvhCNxrHItiu020lyH-dIc1FTT8d1zSxGbOztY130_assertion SIO_000772 12874405 NP400621.RAnvInOkvhCNxrHItiu020lyH-dIc1FTT8d1zSxGbOztY130_provenance.
- NP400621.RAnvInOkvhCNxrHItiu020lyH-dIc1FTT8d1zSxGbOztY130_assertion wasDerivedFrom befree-20140225 NP400621.RAnvInOkvhCNxrHItiu020lyH-dIc1FTT8d1zSxGbOztY130_provenance.
- NP400621.RAnvInOkvhCNxrHItiu020lyH-dIc1FTT8d1zSxGbOztY130_assertion wasGeneratedBy ECO_0000203 NP400621.RAnvInOkvhCNxrHItiu020lyH-dIc1FTT8d1zSxGbOztY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP400621.RAnvInOkvhCNxrHItiu020lyH-dIc1FTT8d1zSxGbOztY130_provenance.