Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP880386.RA3UmvMyVbGl3blfWg4LfR6vORLlPbFBsmCtBeItmE8aQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP880386.RA3UmvMyVbGl3blfWg4LfR6vORLlPbFBsmCtBeItmE8aQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP880386.RA3UmvMyVbGl3blfWg4LfR6vORLlPbFBsmCtBeItmE8aQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP880386.RA3UmvMyVbGl3blfWg4LfR6vORLlPbFBsmCtBeItmE8aQ130_provenance.
- NP880386.RA3UmvMyVbGl3blfWg4LfR6vORLlPbFBsmCtBeItmE8aQ130_assertion description "[Hay-Wells syndrome, caused by mutations in the p63 gene, is an autosomal dominant ectodermal dysplasia with the main features of ankyloblepharon filiforme adnatum, ectodermal defects, and cleft lip/palate, from which the disorder's other name, AEC syndrome, is derived.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP880386.RA3UmvMyVbGl3blfWg4LfR6vORLlPbFBsmCtBeItmE8aQ130_provenance.
- NP880386.RA3UmvMyVbGl3blfWg4LfR6vORLlPbFBsmCtBeItmE8aQ130_assertion evidence source_evidence_literature NP880386.RA3UmvMyVbGl3blfWg4LfR6vORLlPbFBsmCtBeItmE8aQ130_provenance.
- NP880386.RA3UmvMyVbGl3blfWg4LfR6vORLlPbFBsmCtBeItmE8aQ130_assertion SIO_000772 19681128 NP880386.RA3UmvMyVbGl3blfWg4LfR6vORLlPbFBsmCtBeItmE8aQ130_provenance.
- NP880386.RA3UmvMyVbGl3blfWg4LfR6vORLlPbFBsmCtBeItmE8aQ130_assertion wasDerivedFrom befree-20140225 NP880386.RA3UmvMyVbGl3blfWg4LfR6vORLlPbFBsmCtBeItmE8aQ130_provenance.
- NP880386.RA3UmvMyVbGl3blfWg4LfR6vORLlPbFBsmCtBeItmE8aQ130_assertion wasGeneratedBy ECO_0000203 NP880386.RA3UmvMyVbGl3blfWg4LfR6vORLlPbFBsmCtBeItmE8aQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP880386.RA3UmvMyVbGl3blfWg4LfR6vORLlPbFBsmCtBeItmE8aQ130_provenance.