Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1267315.RAYv53A0TdjPHOvnj0QV7zrndIjIzFNd72iTpBOLiwk2s130_assertion> ?p ?o ?g. }
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- NP1267315.RAYv53A0TdjPHOvnj0QV7zrndIjIzFNd72iTpBOLiwk2s130_assertion type Assertion NP1267315.RAYv53A0TdjPHOvnj0QV7zrndIjIzFNd72iTpBOLiwk2s130_head.
- NP1267315.RAYv53A0TdjPHOvnj0QV7zrndIjIzFNd72iTpBOLiwk2s130_assertion description "[Dominant mutations in KAT6A cause intellectual disability with recognizable syndromic features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267315.RAYv53A0TdjPHOvnj0QV7zrndIjIzFNd72iTpBOLiwk2s130_provenance.
- NP1267315.RAYv53A0TdjPHOvnj0QV7zrndIjIzFNd72iTpBOLiwk2s130_assertion evidence source_evidence_literature NP1267315.RAYv53A0TdjPHOvnj0QV7zrndIjIzFNd72iTpBOLiwk2s130_provenance.
- NP1267315.RAYv53A0TdjPHOvnj0QV7zrndIjIzFNd72iTpBOLiwk2s130_assertion SIO_000772 25728777 NP1267315.RAYv53A0TdjPHOvnj0QV7zrndIjIzFNd72iTpBOLiwk2s130_provenance.
- NP1267315.RAYv53A0TdjPHOvnj0QV7zrndIjIzFNd72iTpBOLiwk2s130_assertion wasDerivedFrom befree-2016 NP1267315.RAYv53A0TdjPHOvnj0QV7zrndIjIzFNd72iTpBOLiwk2s130_provenance.
- NP1267315.RAYv53A0TdjPHOvnj0QV7zrndIjIzFNd72iTpBOLiwk2s130_assertion wasGeneratedBy ECO_0000203 NP1267315.RAYv53A0TdjPHOvnj0QV7zrndIjIzFNd72iTpBOLiwk2s130_provenance.