Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1404110.RA130smTWyYqLIA4rq5miiXJIrjX1FuCZV70I-vYvMzeY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1404110.RA130smTWyYqLIA4rq5miiXJIrjX1FuCZV70I-vYvMzeY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1404110.RA130smTWyYqLIA4rq5miiXJIrjX1FuCZV70I-vYvMzeY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1404110.RA130smTWyYqLIA4rq5miiXJIrjX1FuCZV70I-vYvMzeY130_provenance.
- NP1404110.RA130smTWyYqLIA4rq5miiXJIrjX1FuCZV70I-vYvMzeY130_assertion description "[The data suggest that different COL17A1 mutations and their combinations can result in a spectrum of biologic and clinical phenotypes of not only generalized atrophic benign epidermolysis bullosa, but also localized junctional epidermolysis bullosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1404110.RA130smTWyYqLIA4rq5miiXJIrjX1FuCZV70I-vYvMzeY130_provenance.
- NP1404110.RA130smTWyYqLIA4rq5miiXJIrjX1FuCZV70I-vYvMzeY130_assertion evidence source_evidence_literature NP1404110.RA130smTWyYqLIA4rq5miiXJIrjX1FuCZV70I-vYvMzeY130_provenance.
- NP1404110.RA130smTWyYqLIA4rq5miiXJIrjX1FuCZV70I-vYvMzeY130_assertion SIO_000772 9740252 NP1404110.RA130smTWyYqLIA4rq5miiXJIrjX1FuCZV70I-vYvMzeY130_provenance.
- NP1404110.RA130smTWyYqLIA4rq5miiXJIrjX1FuCZV70I-vYvMzeY130_assertion wasDerivedFrom befree-2016 NP1404110.RA130smTWyYqLIA4rq5miiXJIrjX1FuCZV70I-vYvMzeY130_provenance.
- NP1404110.RA130smTWyYqLIA4rq5miiXJIrjX1FuCZV70I-vYvMzeY130_assertion wasGeneratedBy ECO_0000203 NP1404110.RA130smTWyYqLIA4rq5miiXJIrjX1FuCZV70I-vYvMzeY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1404110.RA130smTWyYqLIA4rq5miiXJIrjX1FuCZV70I-vYvMzeY130_provenance.