Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP296386.RASsLAIUL7SdekEWL9S01hBxnwBszgqS_KR3QpDm5EtSM130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP296386.RASsLAIUL7SdekEWL9S01hBxnwBszgqS_KR3QpDm5EtSM130_assertion type Assertion NP296386.RASsLAIUL7SdekEWL9S01hBxnwBszgqS_KR3QpDm5EtSM130_head.
- NP296386.RASsLAIUL7SdekEWL9S01hBxnwBszgqS_KR3QpDm5EtSM130_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." NP296386.RASsLAIUL7SdekEWL9S01hBxnwBszgqS_KR3QpDm5EtSM130_provenance.
- NP296386.RASsLAIUL7SdekEWL9S01hBxnwBszgqS_KR3QpDm5EtSM130_assertion evidence source_evidence_literature NP296386.RASsLAIUL7SdekEWL9S01hBxnwBszgqS_KR3QpDm5EtSM130_provenance.
- NP296386.RASsLAIUL7SdekEWL9S01hBxnwBszgqS_KR3QpDm5EtSM130_assertion SIO_000772 11012604 NP296386.RASsLAIUL7SdekEWL9S01hBxnwBszgqS_KR3QpDm5EtSM130_provenance.
- NP296386.RASsLAIUL7SdekEWL9S01hBxnwBszgqS_KR3QpDm5EtSM130_assertion wasDerivedFrom befree-2016 NP296386.RASsLAIUL7SdekEWL9S01hBxnwBszgqS_KR3QpDm5EtSM130_provenance.
- NP296386.RASsLAIUL7SdekEWL9S01hBxnwBszgqS_KR3QpDm5EtSM130_assertion wasGeneratedBy ECO_0000203 NP296386.RASsLAIUL7SdekEWL9S01hBxnwBszgqS_KR3QpDm5EtSM130_provenance.