Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP857272.RAbPTYRmDrWRaHJjnkV5ApCnBwW3tdC9yMUOON1llwEmY130_assertion> ?p ?o ?g. }
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- NP857272.RAbPTYRmDrWRaHJjnkV5ApCnBwW3tdC9yMUOON1llwEmY130_assertion type Assertion NP857272.RAbPTYRmDrWRaHJjnkV5ApCnBwW3tdC9yMUOON1llwEmY130_head.
- NP857272.RAbPTYRmDrWRaHJjnkV5ApCnBwW3tdC9yMUOON1llwEmY130_assertion wasGeneratedBy ECO_0000203 NP857272.RAbPTYRmDrWRaHJjnkV5ApCnBwW3tdC9yMUOON1llwEmY130_provenance.
- NP857272.RAbPTYRmDrWRaHJjnkV5ApCnBwW3tdC9yMUOON1llwEmY130_assertion wasDerivedFrom befree-20150227 NP857272.RAbPTYRmDrWRaHJjnkV5ApCnBwW3tdC9yMUOON1llwEmY130_provenance.
- NP857272.RAbPTYRmDrWRaHJjnkV5ApCnBwW3tdC9yMUOON1llwEmY130_assertion SIO_000772 16724007 NP857272.RAbPTYRmDrWRaHJjnkV5ApCnBwW3tdC9yMUOON1llwEmY130_provenance.
- NP857272.RAbPTYRmDrWRaHJjnkV5ApCnBwW3tdC9yMUOON1llwEmY130_assertion evidence source_evidence_literature NP857272.RAbPTYRmDrWRaHJjnkV5ApCnBwW3tdC9yMUOON1llwEmY130_provenance.
- NP857272.RAbPTYRmDrWRaHJjnkV5ApCnBwW3tdC9yMUOON1llwEmY130_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." NP857272.RAbPTYRmDrWRaHJjnkV5ApCnBwW3tdC9yMUOON1llwEmY130_provenance.