Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP675038.RABf4YCB6VRVTraadyMaYE_GWtVhkwUrlW_MaH1MCrylY130_assertion> ?p ?o ?g. }
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- NP675038.RABf4YCB6VRVTraadyMaYE_GWtVhkwUrlW_MaH1MCrylY130_assertion type Assertion NP675038.RABf4YCB6VRVTraadyMaYE_GWtVhkwUrlW_MaH1MCrylY130_head.
- NP675038.RABf4YCB6VRVTraadyMaYE_GWtVhkwUrlW_MaH1MCrylY130_assertion description "[Mutations in the p63 gene have recently been delineated as the molecular basis for some cases of the ectrodactyly, ectodermal dysplasia and cleft lip/palate (EEC) syndrome, an autosomal dominant disorder (MIM 129900).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675038.RABf4YCB6VRVTraadyMaYE_GWtVhkwUrlW_MaH1MCrylY130_provenance.
- NP675038.RABf4YCB6VRVTraadyMaYE_GWtVhkwUrlW_MaH1MCrylY130_assertion evidence source_evidence_literature NP675038.RABf4YCB6VRVTraadyMaYE_GWtVhkwUrlW_MaH1MCrylY130_provenance.
- NP675038.RABf4YCB6VRVTraadyMaYE_GWtVhkwUrlW_MaH1MCrylY130_assertion SIO_000772 11012604 NP675038.RABf4YCB6VRVTraadyMaYE_GWtVhkwUrlW_MaH1MCrylY130_provenance.
- NP675038.RABf4YCB6VRVTraadyMaYE_GWtVhkwUrlW_MaH1MCrylY130_assertion wasDerivedFrom befree-20150227 NP675038.RABf4YCB6VRVTraadyMaYE_GWtVhkwUrlW_MaH1MCrylY130_provenance.
- NP675038.RABf4YCB6VRVTraadyMaYE_GWtVhkwUrlW_MaH1MCrylY130_assertion wasGeneratedBy ECO_0000203 NP675038.RABf4YCB6VRVTraadyMaYE_GWtVhkwUrlW_MaH1MCrylY130_provenance.