Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP767921.RA7hX8nOF_A9XYvRRajbCV7quJW7eEV-r-IObuSXXaeTg130_assertion> ?p ?o ?g. }
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- NP767921.RA7hX8nOF_A9XYvRRajbCV7quJW7eEV-r-IObuSXXaeTg130_assertion type Assertion NP767921.RA7hX8nOF_A9XYvRRajbCV7quJW7eEV-r-IObuSXXaeTg130_head.
- NP767921.RA7hX8nOF_A9XYvRRajbCV7quJW7eEV-r-IObuSXXaeTg130_assertion description "[Mutations in the p63 gene are found in a number of human syndromes, including ectrodactyly-ectodermal dysplasia-cleft lip/palate (EEC) syndrome, limb-mammary syndrome (LMS), Hay-Wells syndrome and in non-syndromic split-hand/split-foot malformation (SHFM).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767921.RA7hX8nOF_A9XYvRRajbCV7quJW7eEV-r-IObuSXXaeTg130_provenance.
- NP767921.RA7hX8nOF_A9XYvRRajbCV7quJW7eEV-r-IObuSXXaeTg130_assertion evidence source_evidence_literature NP767921.RA7hX8nOF_A9XYvRRajbCV7quJW7eEV-r-IObuSXXaeTg130_provenance.
- NP767921.RA7hX8nOF_A9XYvRRajbCV7quJW7eEV-r-IObuSXXaeTg130_assertion SIO_000772 11929852 NP767921.RA7hX8nOF_A9XYvRRajbCV7quJW7eEV-r-IObuSXXaeTg130_provenance.
- NP767921.RA7hX8nOF_A9XYvRRajbCV7quJW7eEV-r-IObuSXXaeTg130_assertion wasDerivedFrom befree-20150227 NP767921.RA7hX8nOF_A9XYvRRajbCV7quJW7eEV-r-IObuSXXaeTg130_provenance.
- NP767921.RA7hX8nOF_A9XYvRRajbCV7quJW7eEV-r-IObuSXXaeTg130_assertion wasGeneratedBy ECO_0000203 NP767921.RA7hX8nOF_A9XYvRRajbCV7quJW7eEV-r-IObuSXXaeTg130_provenance.