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- NP799891.RAkYjkuja-JAqAlGAoZSyNWd2G3C8HlNdtG7r7rmChlG0130_assertion type Assertion NP799891.RAkYjkuja-JAqAlGAoZSyNWd2G3C8HlNdtG7r7rmChlG0130_head.
- NP799891.RAkYjkuja-JAqAlGAoZSyNWd2G3C8HlNdtG7r7rmChlG0130_assertion wasGeneratedBy ECO_0000203 NP799891.RAkYjkuja-JAqAlGAoZSyNWd2G3C8HlNdtG7r7rmChlG0130_provenance.
- NP799891.RAkYjkuja-JAqAlGAoZSyNWd2G3C8HlNdtG7r7rmChlG0130_assertion wasDerivedFrom befree-20150227 NP799891.RAkYjkuja-JAqAlGAoZSyNWd2G3C8HlNdtG7r7rmChlG0130_provenance.
- NP799891.RAkYjkuja-JAqAlGAoZSyNWd2G3C8HlNdtG7r7rmChlG0130_assertion SIO_000772 16724007 NP799891.RAkYjkuja-JAqAlGAoZSyNWd2G3C8HlNdtG7r7rmChlG0130_provenance.
- NP799891.RAkYjkuja-JAqAlGAoZSyNWd2G3C8HlNdtG7r7rmChlG0130_assertion evidence source_evidence_literature NP799891.RAkYjkuja-JAqAlGAoZSyNWd2G3C8HlNdtG7r7rmChlG0130_provenance.
- NP799891.RAkYjkuja-JAqAlGAoZSyNWd2G3C8HlNdtG7r7rmChlG0130_assertion description "[Delineation of the ADULT syndrome phenotype due to arginine 298 mutations of the p63 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799891.RAkYjkuja-JAqAlGAoZSyNWd2G3C8HlNdtG7r7rmChlG0130_provenance.