Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP916390.RAAV1o6n2786XG5pey6Xt7ev6vfDoY15mnqKU1rK78xbU130_assertion> ?p ?o ?g. }
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- NP916390.RAAV1o6n2786XG5pey6Xt7ev6vfDoY15mnqKU1rK78xbU130_assertion type Assertion NP916390.RAAV1o6n2786XG5pey6Xt7ev6vfDoY15mnqKU1rK78xbU130_head.
- NP916390.RAAV1o6n2786XG5pey6Xt7ev6vfDoY15mnqKU1rK78xbU130_assertion description "[Sch�pf-Schulz-Passarge syndrome (SSPS; MIM224750) is a rare autosomal recessive form of ectodermal dysplasia that was recently shown to result from mutations in the WNT10A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916390.RAAV1o6n2786XG5pey6Xt7ev6vfDoY15mnqKU1rK78xbU130_provenance.
- NP916390.RAAV1o6n2786XG5pey6Xt7ev6vfDoY15mnqKU1rK78xbU130_assertion evidence source_evidence_literature NP916390.RAAV1o6n2786XG5pey6Xt7ev6vfDoY15mnqKU1rK78xbU130_provenance.
- NP916390.RAAV1o6n2786XG5pey6Xt7ev6vfDoY15mnqKU1rK78xbU130_assertion SIO_000772 21834823 NP916390.RAAV1o6n2786XG5pey6Xt7ev6vfDoY15mnqKU1rK78xbU130_provenance.
- NP916390.RAAV1o6n2786XG5pey6Xt7ev6vfDoY15mnqKU1rK78xbU130_assertion wasDerivedFrom befree-2016 NP916390.RAAV1o6n2786XG5pey6Xt7ev6vfDoY15mnqKU1rK78xbU130_provenance.
- NP916390.RAAV1o6n2786XG5pey6Xt7ev6vfDoY15mnqKU1rK78xbU130_assertion wasGeneratedBy ECO_0000203 NP916390.RAAV1o6n2786XG5pey6Xt7ev6vfDoY15mnqKU1rK78xbU130_provenance.