Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP948965.RAKvdYyUJlcdssXgF351KpGQ3UuhjqzelgOoyPPWCc4r0130_assertion> ?p ?o ?g. }
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- NP948965.RAKvdYyUJlcdssXgF351KpGQ3UuhjqzelgOoyPPWCc4r0130_assertion type Assertion NP948965.RAKvdYyUJlcdssXgF351KpGQ3UuhjqzelgOoyPPWCc4r0130_head.
- NP948965.RAKvdYyUJlcdssXgF351KpGQ3UuhjqzelgOoyPPWCc4r0130_assertion wasGeneratedBy ECO_0000203 NP948965.RAKvdYyUJlcdssXgF351KpGQ3UuhjqzelgOoyPPWCc4r0130_provenance.
- NP948965.RAKvdYyUJlcdssXgF351KpGQ3UuhjqzelgOoyPPWCc4r0130_assertion wasDerivedFrom befree-20150227 NP948965.RAKvdYyUJlcdssXgF351KpGQ3UuhjqzelgOoyPPWCc4r0130_provenance.
- NP948965.RAKvdYyUJlcdssXgF351KpGQ3UuhjqzelgOoyPPWCc4r0130_assertion SIO_000772 17847007 NP948965.RAKvdYyUJlcdssXgF351KpGQ3UuhjqzelgOoyPPWCc4r0130_provenance.
- NP948965.RAKvdYyUJlcdssXgF351KpGQ3UuhjqzelgOoyPPWCc4r0130_assertion evidence source_evidence_literature NP948965.RAKvdYyUJlcdssXgF351KpGQ3UuhjqzelgOoyPPWCc4r0130_provenance.
- NP948965.RAKvdYyUJlcdssXgF351KpGQ3UuhjqzelgOoyPPWCc4r0130_assertion description "[This is the first report to our knowledge of a human phenotype resulting from a mutation in WNT10A, and it is the first demonstration of an ectodermal dysplasia caused by an altered WNT signaling pathway, expanding the list of WNT-related diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948965.RAKvdYyUJlcdssXgF351KpGQ3UuhjqzelgOoyPPWCc4r0130_provenance.