Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_provenance.
- NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_assertion description "[Mutations in the p63 gene have been identified in five human disorders characterized by varying degrees of limb anomalies, ectodermal dysplasia, and facial clefts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_provenance.
- NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_assertion evidence source_evidence_literature NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_provenance.
- NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_assertion SIO_000772 16190990 NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_provenance.
- NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_assertion wasDerivedFrom befree-20150227 NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_provenance.
- NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_assertion wasGeneratedBy ECO_0000203 NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP799807.RA6nmyAPjfAiXqf0wcIH4JOUItP8kyifOGg7ymE7LX8Wo130_provenance.