Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP6695.RAUQ7oDDSEhxuSI-kUVSw86JW_RicwcvK5oeAQEaV_uZg130_assertion> ?p ?o ?g. }
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- NP6695.RAUQ7oDDSEhxuSI-kUVSw86JW_RicwcvK5oeAQEaV_uZg130_assertion type Assertion NP6695.RAUQ7oDDSEhxuSI-kUVSw86JW_RicwcvK5oeAQEaV_uZg130_head.
- NP6695.RAUQ7oDDSEhxuSI-kUVSw86JW_RicwcvK5oeAQEaV_uZg130_assertion wasGeneratedBy ECO_0000218 NP6695.RAUQ7oDDSEhxuSI-kUVSw86JW_RicwcvK5oeAQEaV_uZg130_provenance.
- NP6695.RAUQ7oDDSEhxuSI-kUVSw86JW_RicwcvK5oeAQEaV_uZg130_assertion wasDerivedFrom uniprot-20130724 NP6695.RAUQ7oDDSEhxuSI-kUVSw86JW_RicwcvK5oeAQEaV_uZg130_provenance.
- NP6695.RAUQ7oDDSEhxuSI-kUVSw86JW_RicwcvK5oeAQEaV_uZg130_assertion SIO_000772 11159940 NP6695.RAUQ7oDDSEhxuSI-kUVSw86JW_RicwcvK5oeAQEaV_uZg130_provenance.
- NP6695.RAUQ7oDDSEhxuSI-kUVSw86JW_RicwcvK5oeAQEaV_uZg130_assertion evidence source_evidence_curated NP6695.RAUQ7oDDSEhxuSI-kUVSw86JW_RicwcvK5oeAQEaV_uZg130_provenance.
- NP6695.RAUQ7oDDSEhxuSI-kUVSw86JW_RicwcvK5oeAQEaV_uZg130_assertion description "[Hay-Wells syndrome is caused by heterozygous missense mutations in the SAM domain of p63.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6695.RAUQ7oDDSEhxuSI-kUVSw86JW_RicwcvK5oeAQEaV_uZg130_provenance.