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- source_evidence_literature type ECO_0000212 NP342836.RAqI7XmUfznnZKZq7PcKP-fKPX_VxkmgIRjTaLna1Qxc0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP342836.RAqI7XmUfznnZKZq7PcKP-fKPX_VxkmgIRjTaLna1Qxc0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP342836.RAqI7XmUfznnZKZq7PcKP-fKPX_VxkmgIRjTaLna1Qxc0130_provenance.
- NP342836.RAqI7XmUfznnZKZq7PcKP-fKPX_VxkmgIRjTaLna1Qxc0130_assertion description "[Mutations in the human ARX gene have been shown to cause nonsyndromic X-linked mental retardation (MRX) as well as syndromic forms such as X-linked lissencephaly with abnormal genitalia (XLAG), Partington syndrome and X-linked infantile spasm.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP342836.RAqI7XmUfznnZKZq7PcKP-fKPX_VxkmgIRjTaLna1Qxc0130_provenance.
- NP342836.RAqI7XmUfznnZKZq7PcKP-fKPX_VxkmgIRjTaLna1Qxc0130_assertion evidence source_evidence_literature NP342836.RAqI7XmUfznnZKZq7PcKP-fKPX_VxkmgIRjTaLna1Qxc0130_provenance.
- NP342836.RAqI7XmUfznnZKZq7PcKP-fKPX_VxkmgIRjTaLna1Qxc0130_assertion SIO_000772 16235064 NP342836.RAqI7XmUfznnZKZq7PcKP-fKPX_VxkmgIRjTaLna1Qxc0130_provenance.
- NP342836.RAqI7XmUfznnZKZq7PcKP-fKPX_VxkmgIRjTaLna1Qxc0130_assertion wasDerivedFrom befree-20140225 NP342836.RAqI7XmUfznnZKZq7PcKP-fKPX_VxkmgIRjTaLna1Qxc0130_provenance.
- NP342836.RAqI7XmUfznnZKZq7PcKP-fKPX_VxkmgIRjTaLna1Qxc0130_assertion wasGeneratedBy ECO_0000203 NP342836.RAqI7XmUfznnZKZq7PcKP-fKPX_VxkmgIRjTaLna1Qxc0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP342836.RAqI7XmUfznnZKZq7PcKP-fKPX_VxkmgIRjTaLna1Qxc0130_provenance.