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- NP674825.RAchRIto2eaOFJNF-_G2p38ihf07xKXppvGpBqa_qxBDo130_assertion type Assertion NP674825.RAchRIto2eaOFJNF-_G2p38ihf07xKXppvGpBqa_qxBDo130_head.
- NP674825.RAchRIto2eaOFJNF-_G2p38ihf07xKXppvGpBqa_qxBDo130_assertion wasGeneratedBy ECO_0000203 NP674825.RAchRIto2eaOFJNF-_G2p38ihf07xKXppvGpBqa_qxBDo130_provenance.
- NP674825.RAchRIto2eaOFJNF-_G2p38ihf07xKXppvGpBqa_qxBDo130_assertion wasDerivedFrom befree-20150227 NP674825.RAchRIto2eaOFJNF-_G2p38ihf07xKXppvGpBqa_qxBDo130_provenance.
- NP674825.RAchRIto2eaOFJNF-_G2p38ihf07xKXppvGpBqa_qxBDo130_assertion SIO_000772 17224651 NP674825.RAchRIto2eaOFJNF-_G2p38ihf07xKXppvGpBqa_qxBDo130_provenance.
- NP674825.RAchRIto2eaOFJNF-_G2p38ihf07xKXppvGpBqa_qxBDo130_assertion evidence source_evidence_literature NP674825.RAchRIto2eaOFJNF-_G2p38ihf07xKXppvGpBqa_qxBDo130_provenance.
- NP674825.RAchRIto2eaOFJNF-_G2p38ihf07xKXppvGpBqa_qxBDo130_assertion description "[Heterozygous mutations in the transcription factor gene p63 are causative for several syndromes, with ectodermal dysplasia, orofacial clefting and limb malformations as the key characteristics.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP674825.RAchRIto2eaOFJNF-_G2p38ihf07xKXppvGpBqa_qxBDo130_provenance.