Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP978218.RAPJ4YLvFMpDCv0g55-fj9w85Zywi8ySo5RvjejoTW4OE130_assertion> ?p ?o ?g. }
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- NP978218.RAPJ4YLvFMpDCv0g55-fj9w85Zywi8ySo5RvjejoTW4OE130_assertion type Assertion NP978218.RAPJ4YLvFMpDCv0g55-fj9w85Zywi8ySo5RvjejoTW4OE130_head.
- 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.