Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP578163.RAOUDbmxkgva0jPFxQLn95KXUaG0Ic87jNCr-eqIdSIEE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP578163.RAOUDbmxkgva0jPFxQLn95KXUaG0Ic87jNCr-eqIdSIEE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP578163.RAOUDbmxkgva0jPFxQLn95KXUaG0Ic87jNCr-eqIdSIEE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP578163.RAOUDbmxkgva0jPFxQLn95KXUaG0Ic87jNCr-eqIdSIEE130_provenance.
- NP578163.RAOUDbmxkgva0jPFxQLn95KXUaG0Ic87jNCr-eqIdSIEE130_assertion description "[We recently identified mutations of ARX in nine genotypic males with X-linked lissencephaly with abnormal genitalia (XLAG), and in several female relatives with isolated agenesis of the corpus callosum (ACC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP578163.RAOUDbmxkgva0jPFxQLn95KXUaG0Ic87jNCr-eqIdSIEE130_provenance.
- NP578163.RAOUDbmxkgva0jPFxQLn95KXUaG0Ic87jNCr-eqIdSIEE130_assertion evidence source_evidence_literature NP578163.RAOUDbmxkgva0jPFxQLn95KXUaG0Ic87jNCr-eqIdSIEE130_provenance.
- NP578163.RAOUDbmxkgva0jPFxQLn95KXUaG0Ic87jNCr-eqIdSIEE130_assertion SIO_000772 14722918 NP578163.RAOUDbmxkgva0jPFxQLn95KXUaG0Ic87jNCr-eqIdSIEE130_provenance.
- NP578163.RAOUDbmxkgva0jPFxQLn95KXUaG0Ic87jNCr-eqIdSIEE130_assertion wasDerivedFrom befree-20140225 NP578163.RAOUDbmxkgva0jPFxQLn95KXUaG0Ic87jNCr-eqIdSIEE130_provenance.
- NP578163.RAOUDbmxkgva0jPFxQLn95KXUaG0Ic87jNCr-eqIdSIEE130_assertion wasGeneratedBy ECO_0000203 NP578163.RAOUDbmxkgva0jPFxQLn95KXUaG0Ic87jNCr-eqIdSIEE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP578163.RAOUDbmxkgva0jPFxQLn95KXUaG0Ic87jNCr-eqIdSIEE130_provenance.