Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP747812.RAFeDTz8vs7_351ggkSa3v9yBPbVFVjIoQ_oCLL2_ugUY130_assertion> ?p ?o ?g. }
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- NP747812.RAFeDTz8vs7_351ggkSa3v9yBPbVFVjIoQ_oCLL2_ugUY130_assertion type Assertion NP747812.RAFeDTz8vs7_351ggkSa3v9yBPbVFVjIoQ_oCLL2_ugUY130_head.
- NP747812.RAFeDTz8vs7_351ggkSa3v9yBPbVFVjIoQ_oCLL2_ugUY130_assertion description "[WNT10A mutations are a frequent cause of a broad spectrum of ectodermal dysplasias with sex-biased manifestation pattern in heterozygotes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP747812.RAFeDTz8vs7_351ggkSa3v9yBPbVFVjIoQ_oCLL2_ugUY130_provenance.
- NP747812.RAFeDTz8vs7_351ggkSa3v9yBPbVFVjIoQ_oCLL2_ugUY130_assertion evidence source_evidence_literature NP747812.RAFeDTz8vs7_351ggkSa3v9yBPbVFVjIoQ_oCLL2_ugUY130_provenance.
- NP747812.RAFeDTz8vs7_351ggkSa3v9yBPbVFVjIoQ_oCLL2_ugUY130_assertion SIO_000772 19559398 NP747812.RAFeDTz8vs7_351ggkSa3v9yBPbVFVjIoQ_oCLL2_ugUY130_provenance.
- NP747812.RAFeDTz8vs7_351ggkSa3v9yBPbVFVjIoQ_oCLL2_ugUY130_assertion wasDerivedFrom befree-2016 NP747812.RAFeDTz8vs7_351ggkSa3v9yBPbVFVjIoQ_oCLL2_ugUY130_provenance.
- NP747812.RAFeDTz8vs7_351ggkSa3v9yBPbVFVjIoQ_oCLL2_ugUY130_assertion wasGeneratedBy ECO_0000203 NP747812.RAFeDTz8vs7_351ggkSa3v9yBPbVFVjIoQ_oCLL2_ugUY130_provenance.