Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP296378.RATD4EJaEqsTJ8nKxVo2y2NHqguSi9HF5G9qw4D6ljrNI130_assertion> ?p ?o ?g. }
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- NP296378.RATD4EJaEqsTJ8nKxVo2y2NHqguSi9HF5G9qw4D6ljrNI130_assertion type Assertion NP296378.RATD4EJaEqsTJ8nKxVo2y2NHqguSi9HF5G9qw4D6ljrNI130_head.
- NP296378.RATD4EJaEqsTJ8nKxVo2y2NHqguSi9HF5G9qw4D6ljrNI130_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." NP296378.RATD4EJaEqsTJ8nKxVo2y2NHqguSi9HF5G9qw4D6ljrNI130_provenance.
- NP296378.RATD4EJaEqsTJ8nKxVo2y2NHqguSi9HF5G9qw4D6ljrNI130_assertion evidence source_evidence_literature NP296378.RATD4EJaEqsTJ8nKxVo2y2NHqguSi9HF5G9qw4D6ljrNI130_provenance.
- NP296378.RATD4EJaEqsTJ8nKxVo2y2NHqguSi9HF5G9qw4D6ljrNI130_assertion SIO_000772 11012604 NP296378.RATD4EJaEqsTJ8nKxVo2y2NHqguSi9HF5G9qw4D6ljrNI130_provenance.
- NP296378.RATD4EJaEqsTJ8nKxVo2y2NHqguSi9HF5G9qw4D6ljrNI130_assertion wasDerivedFrom befree-2016 NP296378.RATD4EJaEqsTJ8nKxVo2y2NHqguSi9HF5G9qw4D6ljrNI130_provenance.
- NP296378.RATD4EJaEqsTJ8nKxVo2y2NHqguSi9HF5G9qw4D6ljrNI130_assertion wasGeneratedBy ECO_0000203 NP296378.RATD4EJaEqsTJ8nKxVo2y2NHqguSi9HF5G9qw4D6ljrNI130_provenance.