Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1367176.RABrB1UpRGgI4Swns7TX_ULDvJuDRXq-vMaiej01lqRQM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1367176.RABrB1UpRGgI4Swns7TX_ULDvJuDRXq-vMaiej01lqRQM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1367176.RABrB1UpRGgI4Swns7TX_ULDvJuDRXq-vMaiej01lqRQM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1367176.RABrB1UpRGgI4Swns7TX_ULDvJuDRXq-vMaiej01lqRQM130_provenance.
- NP1367176.RABrB1UpRGgI4Swns7TX_ULDvJuDRXq-vMaiej01lqRQM130_assertion description "[This year, the first mutations in a keratin-associated protein, plectin, were shown to cause a variant of epidermolysis bullosa associated with late-onset muscular dystrophy (MD-EBS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1367176.RABrB1UpRGgI4Swns7TX_ULDvJuDRXq-vMaiej01lqRQM130_provenance.
- NP1367176.RABrB1UpRGgI4Swns7TX_ULDvJuDRXq-vMaiej01lqRQM130_assertion evidence source_evidence_literature NP1367176.RABrB1UpRGgI4Swns7TX_ULDvJuDRXq-vMaiej01lqRQM130_provenance.
- NP1367176.RABrB1UpRGgI4Swns7TX_ULDvJuDRXq-vMaiej01lqRQM130_assertion SIO_000772 9028791 NP1367176.RABrB1UpRGgI4Swns7TX_ULDvJuDRXq-vMaiej01lqRQM130_provenance.
- NP1367176.RABrB1UpRGgI4Swns7TX_ULDvJuDRXq-vMaiej01lqRQM130_assertion wasDerivedFrom befree-2016 NP1367176.RABrB1UpRGgI4Swns7TX_ULDvJuDRXq-vMaiej01lqRQM130_provenance.
- NP1367176.RABrB1UpRGgI4Swns7TX_ULDvJuDRXq-vMaiej01lqRQM130_assertion wasGeneratedBy ECO_0000203 NP1367176.RABrB1UpRGgI4Swns7TX_ULDvJuDRXq-vMaiej01lqRQM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1367176.RABrB1UpRGgI4Swns7TX_ULDvJuDRXq-vMaiej01lqRQM130_provenance.