Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP701688.RAtUCdUn24LD64sM_v0cQQMTyj2K2tUr6GFt0IU_VLrXc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP701688.RAtUCdUn24LD64sM_v0cQQMTyj2K2tUr6GFt0IU_VLrXc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP701688.RAtUCdUn24LD64sM_v0cQQMTyj2K2tUr6GFt0IU_VLrXc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP701688.RAtUCdUn24LD64sM_v0cQQMTyj2K2tUr6GFt0IU_VLrXc130_provenance.
- NP701688.RAtUCdUn24LD64sM_v0cQQMTyj2K2tUr6GFt0IU_VLrXc130_assertion description "[Pachyonychia congenita (PC) is a rare autosomal dominant keratin disorder, subdivided into two major variants, PC-1 and PC-2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP701688.RAtUCdUn24LD64sM_v0cQQMTyj2K2tUr6GFt0IU_VLrXc130_provenance.
- NP701688.RAtUCdUn24LD64sM_v0cQQMTyj2K2tUr6GFt0IU_VLrXc130_assertion evidence source_evidence_literature NP701688.RAtUCdUn24LD64sM_v0cQQMTyj2K2tUr6GFt0IU_VLrXc130_provenance.
- NP701688.RAtUCdUn24LD64sM_v0cQQMTyj2K2tUr6GFt0IU_VLrXc130_assertion SIO_000772 17719747 NP701688.RAtUCdUn24LD64sM_v0cQQMTyj2K2tUr6GFt0IU_VLrXc130_provenance.
- NP701688.RAtUCdUn24LD64sM_v0cQQMTyj2K2tUr6GFt0IU_VLrXc130_assertion wasDerivedFrom befree-20140225 NP701688.RAtUCdUn24LD64sM_v0cQQMTyj2K2tUr6GFt0IU_VLrXc130_provenance.
- NP701688.RAtUCdUn24LD64sM_v0cQQMTyj2K2tUr6GFt0IU_VLrXc130_assertion wasGeneratedBy ECO_0000203 NP701688.RAtUCdUn24LD64sM_v0cQQMTyj2K2tUr6GFt0IU_VLrXc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP701688.RAtUCdUn24LD64sM_v0cQQMTyj2K2tUr6GFt0IU_VLrXc130_provenance.