Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP296388.RA5wlh1CTfY16efbba1KOe1zICPQ0l4BvA1XX6vqgvVFo130_assertion> ?p ?o ?g. }
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- NP296388.RA5wlh1CTfY16efbba1KOe1zICPQ0l4BvA1XX6vqgvVFo130_assertion type Assertion NP296388.RA5wlh1CTfY16efbba1KOe1zICPQ0l4BvA1XX6vqgvVFo130_head.
- NP296388.RA5wlh1CTfY16efbba1KOe1zICPQ0l4BvA1XX6vqgvVFo130_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." NP296388.RA5wlh1CTfY16efbba1KOe1zICPQ0l4BvA1XX6vqgvVFo130_provenance.
- NP296388.RA5wlh1CTfY16efbba1KOe1zICPQ0l4BvA1XX6vqgvVFo130_assertion evidence source_evidence_literature NP296388.RA5wlh1CTfY16efbba1KOe1zICPQ0l4BvA1XX6vqgvVFo130_provenance.
- NP296388.RA5wlh1CTfY16efbba1KOe1zICPQ0l4BvA1XX6vqgvVFo130_assertion SIO_000772 11012604 NP296388.RA5wlh1CTfY16efbba1KOe1zICPQ0l4BvA1XX6vqgvVFo130_provenance.
- NP296388.RA5wlh1CTfY16efbba1KOe1zICPQ0l4BvA1XX6vqgvVFo130_assertion wasDerivedFrom befree-2016 NP296388.RA5wlh1CTfY16efbba1KOe1zICPQ0l4BvA1XX6vqgvVFo130_provenance.
- NP296388.RA5wlh1CTfY16efbba1KOe1zICPQ0l4BvA1XX6vqgvVFo130_assertion wasGeneratedBy ECO_0000203 NP296388.RA5wlh1CTfY16efbba1KOe1zICPQ0l4BvA1XX6vqgvVFo130_provenance.