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- NP584474.RAL14RlKYdt2d-sgWi1gobMSUnlxowp1NlceLmMmXp_0g130_assertion type Assertion NP584474.RAL14RlKYdt2d-sgWi1gobMSUnlxowp1NlceLmMmXp_0g130_head.
- NP584474.RAL14RlKYdt2d-sgWi1gobMSUnlxowp1NlceLmMmXp_0g130_assertion wasGeneratedBy ECO_0000203 NP584474.RAL14RlKYdt2d-sgWi1gobMSUnlxowp1NlceLmMmXp_0g130_provenance.
- NP584474.RAL14RlKYdt2d-sgWi1gobMSUnlxowp1NlceLmMmXp_0g130_assertion wasDerivedFrom befree-20140225 NP584474.RAL14RlKYdt2d-sgWi1gobMSUnlxowp1NlceLmMmXp_0g130_provenance.
- NP584474.RAL14RlKYdt2d-sgWi1gobMSUnlxowp1NlceLmMmXp_0g130_assertion SIO_000772 19239083 NP584474.RAL14RlKYdt2d-sgWi1gobMSUnlxowp1NlceLmMmXp_0g130_provenance.
- NP584474.RAL14RlKYdt2d-sgWi1gobMSUnlxowp1NlceLmMmXp_0g130_assertion evidence source_evidence_literature NP584474.RAL14RlKYdt2d-sgWi1gobMSUnlxowp1NlceLmMmXp_0g130_provenance.
- NP584474.RAL14RlKYdt2d-sgWi1gobMSUnlxowp1NlceLmMmXp_0g130_assertion description "[The ankyloblepharon-ectodermal defects-cleft lip and palate (Hay-Wells or AEC) and the Rapp-Hodgkin syndrome (RHS) are rare autosomal dominant ectodermal dysplasias due to mutations in the transcription factor gene P63.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584474.RAL14RlKYdt2d-sgWi1gobMSUnlxowp1NlceLmMmXp_0g130_provenance.