Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP835542.RA8zcdlpIvOHeeNiiC3v0bZLpcFxbVuq6EkGUYovSd9PI130_assertion> ?p ?o ?g. }
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- NP835542.RA8zcdlpIvOHeeNiiC3v0bZLpcFxbVuq6EkGUYovSd9PI130_assertion type Assertion NP835542.RA8zcdlpIvOHeeNiiC3v0bZLpcFxbVuq6EkGUYovSd9PI130_head.
- NP835542.RA8zcdlpIvOHeeNiiC3v0bZLpcFxbVuq6EkGUYovSd9PI130_assertion description "[This finding makes the ARX dup24 mutation the most common mutation in nonsyndromic XLMR families linked to Xp22.1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835542.RA8zcdlpIvOHeeNiiC3v0bZLpcFxbVuq6EkGUYovSd9PI130_provenance.
- NP835542.RA8zcdlpIvOHeeNiiC3v0bZLpcFxbVuq6EkGUYovSd9PI130_assertion evidence source_evidence_literature NP835542.RA8zcdlpIvOHeeNiiC3v0bZLpcFxbVuq6EkGUYovSd9PI130_provenance.
- NP835542.RA8zcdlpIvOHeeNiiC3v0bZLpcFxbVuq6EkGUYovSd9PI130_assertion SIO_000772 15850492 NP835542.RA8zcdlpIvOHeeNiiC3v0bZLpcFxbVuq6EkGUYovSd9PI130_provenance.
- NP835542.RA8zcdlpIvOHeeNiiC3v0bZLpcFxbVuq6EkGUYovSd9PI130_assertion wasDerivedFrom befree-20150227 NP835542.RA8zcdlpIvOHeeNiiC3v0bZLpcFxbVuq6EkGUYovSd9PI130_provenance.
- NP835542.RA8zcdlpIvOHeeNiiC3v0bZLpcFxbVuq6EkGUYovSd9PI130_assertion wasGeneratedBy ECO_0000203 NP835542.RA8zcdlpIvOHeeNiiC3v0bZLpcFxbVuq6EkGUYovSd9PI130_provenance.