Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP675028.RArBx9H5jV-vAKem1Pu7KYsYNhlt4XLlzPPRxDYlpZMsE130_assertion> ?p ?o ?g. }
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- NP675028.RArBx9H5jV-vAKem1Pu7KYsYNhlt4XLlzPPRxDYlpZMsE130_assertion type Assertion NP675028.RArBx9H5jV-vAKem1Pu7KYsYNhlt4XLlzPPRxDYlpZMsE130_head.
- NP675028.RArBx9H5jV-vAKem1Pu7KYsYNhlt4XLlzPPRxDYlpZMsE130_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." NP675028.RArBx9H5jV-vAKem1Pu7KYsYNhlt4XLlzPPRxDYlpZMsE130_provenance.
- NP675028.RArBx9H5jV-vAKem1Pu7KYsYNhlt4XLlzPPRxDYlpZMsE130_assertion evidence source_evidence_literature NP675028.RArBx9H5jV-vAKem1Pu7KYsYNhlt4XLlzPPRxDYlpZMsE130_provenance.
- NP675028.RArBx9H5jV-vAKem1Pu7KYsYNhlt4XLlzPPRxDYlpZMsE130_assertion SIO_000772 11012604 NP675028.RArBx9H5jV-vAKem1Pu7KYsYNhlt4XLlzPPRxDYlpZMsE130_provenance.
- NP675028.RArBx9H5jV-vAKem1Pu7KYsYNhlt4XLlzPPRxDYlpZMsE130_assertion wasDerivedFrom befree-20150227 NP675028.RArBx9H5jV-vAKem1Pu7KYsYNhlt4XLlzPPRxDYlpZMsE130_provenance.
- NP675028.RArBx9H5jV-vAKem1Pu7KYsYNhlt4XLlzPPRxDYlpZMsE130_assertion wasGeneratedBy ECO_0000203 NP675028.RArBx9H5jV-vAKem1Pu7KYsYNhlt4XLlzPPRxDYlpZMsE130_provenance.