Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP588971.RAWHpmz8GVShMwWrisyWl5cqdp7hEunJ0hqr00yUF7Dnk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP588971.RAWHpmz8GVShMwWrisyWl5cqdp7hEunJ0hqr00yUF7Dnk130_assertion type Assertion NP588971.RAWHpmz8GVShMwWrisyWl5cqdp7hEunJ0hqr00yUF7Dnk130_head.
- NP588971.RAWHpmz8GVShMwWrisyWl5cqdp7hEunJ0hqr00yUF7Dnk130_assertion wasGeneratedBy ECO_0000203 NP588971.RAWHpmz8GVShMwWrisyWl5cqdp7hEunJ0hqr00yUF7Dnk130_provenance.
- NP588971.RAWHpmz8GVShMwWrisyWl5cqdp7hEunJ0hqr00yUF7Dnk130_assertion wasDerivedFrom befree-2016 NP588971.RAWHpmz8GVShMwWrisyWl5cqdp7hEunJ0hqr00yUF7Dnk130_provenance.
- NP588971.RAWHpmz8GVShMwWrisyWl5cqdp7hEunJ0hqr00yUF7Dnk130_assertion SIO_000772 17224651 NP588971.RAWHpmz8GVShMwWrisyWl5cqdp7hEunJ0hqr00yUF7Dnk130_provenance.
- NP588971.RAWHpmz8GVShMwWrisyWl5cqdp7hEunJ0hqr00yUF7Dnk130_assertion evidence source_evidence_literature NP588971.RAWHpmz8GVShMwWrisyWl5cqdp7hEunJ0hqr00yUF7Dnk130_provenance.
- NP588971.RAWHpmz8GVShMwWrisyWl5cqdp7hEunJ0hqr00yUF7Dnk130_assertion description "[Heterozygous mutations in the transcription factor gene p63 are causative for several syndromes, with ectodermal dysplasia, orofacial clefting and limb malformations as the key characteristics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588971.RAWHpmz8GVShMwWrisyWl5cqdp7hEunJ0hqr00yUF7Dnk130_provenance.