Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1052826.RAoQz-G8pIf0otMe2PiUvVGmwzGM5ToDVzugMAVdfj2yY130_assertion> ?p ?o ?g. }
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- NP1052826.RAoQz-G8pIf0otMe2PiUvVGmwzGM5ToDVzugMAVdfj2yY130_assertion type Assertion NP1052826.RAoQz-G8pIf0otMe2PiUvVGmwzGM5ToDVzugMAVdfj2yY130_head.
- NP1052826.RAoQz-G8pIf0otMe2PiUvVGmwzGM5ToDVzugMAVdfj2yY130_assertion description "[The most frequent p63 mutation syndrome is the EEC syndrome, characterized by ectrodactyly, ectodermal dysplasia and cleft lip/palate.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1052826.RAoQz-G8pIf0otMe2PiUvVGmwzGM5ToDVzugMAVdfj2yY130_provenance.
- NP1052826.RAoQz-G8pIf0otMe2PiUvVGmwzGM5ToDVzugMAVdfj2yY130_assertion evidence source_evidence_literature NP1052826.RAoQz-G8pIf0otMe2PiUvVGmwzGM5ToDVzugMAVdfj2yY130_provenance.
- NP1052826.RAoQz-G8pIf0otMe2PiUvVGmwzGM5ToDVzugMAVdfj2yY130_assertion SIO_000772 23407076 NP1052826.RAoQz-G8pIf0otMe2PiUvVGmwzGM5ToDVzugMAVdfj2yY130_provenance.
- NP1052826.RAoQz-G8pIf0otMe2PiUvVGmwzGM5ToDVzugMAVdfj2yY130_assertion wasDerivedFrom befree-2016 NP1052826.RAoQz-G8pIf0otMe2PiUvVGmwzGM5ToDVzugMAVdfj2yY130_provenance.
- NP1052826.RAoQz-G8pIf0otMe2PiUvVGmwzGM5ToDVzugMAVdfj2yY130_assertion wasGeneratedBy ECO_0000203 NP1052826.RAoQz-G8pIf0otMe2PiUvVGmwzGM5ToDVzugMAVdfj2yY130_provenance.