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- source_evidence_literature type ECO_0000212 NP978218.RAPJ4YLvFMpDCv0g55-fj9w85Zywi8ySo5RvjejoTW4OE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978218.RAPJ4YLvFMpDCv0g55-fj9w85Zywi8ySo5RvjejoTW4OE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978218.RAPJ4YLvFMpDCv0g55-fj9w85Zywi8ySo5RvjejoTW4OE130_provenance.
- NP978218.RAPJ4YLvFMpDCv0g55-fj9w85Zywi8ySo5RvjejoTW4OE130_assertion description "[The Aristaless-related homeobox gene (ARX) is one of the most frequently mutated genes in a spectrum of X-chromosome phenotypes with intellectual disability (ID) as their cardinal feature.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978218.RAPJ4YLvFMpDCv0g55-fj9w85Zywi8ySo5RvjejoTW4OE130_provenance.
- NP978218.RAPJ4YLvFMpDCv0g55-fj9w85Zywi8ySo5RvjejoTW4OE130_assertion evidence source_evidence_literature NP978218.RAPJ4YLvFMpDCv0g55-fj9w85Zywi8ySo5RvjejoTW4OE130_provenance.
- NP978218.RAPJ4YLvFMpDCv0g55-fj9w85Zywi8ySo5RvjejoTW4OE130_assertion SIO_000772 20506206 NP978218.RAPJ4YLvFMpDCv0g55-fj9w85Zywi8ySo5RvjejoTW4OE130_provenance.
- NP978218.RAPJ4YLvFMpDCv0g55-fj9w85Zywi8ySo5RvjejoTW4OE130_assertion wasDerivedFrom befree-20150227 NP978218.RAPJ4YLvFMpDCv0g55-fj9w85Zywi8ySo5RvjejoTW4OE130_provenance.
- NP978218.RAPJ4YLvFMpDCv0g55-fj9w85Zywi8ySo5RvjejoTW4OE130_assertion wasGeneratedBy ECO_0000203 NP978218.RAPJ4YLvFMpDCv0g55-fj9w85Zywi8ySo5RvjejoTW4OE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978218.RAPJ4YLvFMpDCv0g55-fj9w85Zywi8ySo5RvjejoTW4OE130_provenance.