Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP617342.RAOAmNer82sNbMVEWv5km69bSOV4U6TyP_WUcAt-tf3GQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP617342.RAOAmNer82sNbMVEWv5km69bSOV4U6TyP_WUcAt-tf3GQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP617342.RAOAmNer82sNbMVEWv5km69bSOV4U6TyP_WUcAt-tf3GQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP617342.RAOAmNer82sNbMVEWv5km69bSOV4U6TyP_WUcAt-tf3GQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP617342.RAOAmNer82sNbMVEWv5km69bSOV4U6TyP_WUcAt-tf3GQ130_provenance.
- NP617342.RAOAmNer82sNbMVEWv5km69bSOV4U6TyP_WUcAt-tf3GQ130_assertion wasGeneratedBy ECO_0000203 NP617342.RAOAmNer82sNbMVEWv5km69bSOV4U6TyP_WUcAt-tf3GQ130_provenance.
- NP617342.RAOAmNer82sNbMVEWv5km69bSOV4U6TyP_WUcAt-tf3GQ130_assertion wasDerivedFrom befree-2016 NP617342.RAOAmNer82sNbMVEWv5km69bSOV4U6TyP_WUcAt-tf3GQ130_provenance.
- NP617342.RAOAmNer82sNbMVEWv5km69bSOV4U6TyP_WUcAt-tf3GQ130_assertion SIO_000772 17597066 NP617342.RAOAmNer82sNbMVEWv5km69bSOV4U6TyP_WUcAt-tf3GQ130_provenance.
- NP617342.RAOAmNer82sNbMVEWv5km69bSOV4U6TyP_WUcAt-tf3GQ130_assertion evidence source_evidence_literature NP617342.RAOAmNer82sNbMVEWv5km69bSOV4U6TyP_WUcAt-tf3GQ130_provenance.
- NP617342.RAOAmNer82sNbMVEWv5km69bSOV4U6TyP_WUcAt-tf3GQ130_assertion description "[Loss of one copy of the human ATP2C1 gene, encoding SPCA1 (secretory pathway Ca(2+)-ATPase isoform 1), causes Hailey-Hailey disease, a skin disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP617342.RAOAmNer82sNbMVEWv5km69bSOV4U6TyP_WUcAt-tf3GQ130_provenance.