Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1327156.RAbgnezefUyTRP7otdO0mFpwEBG50_MCWQg6stTTbpR6c130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1327156.RAbgnezefUyTRP7otdO0mFpwEBG50_MCWQg6stTTbpR6c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1327156.RAbgnezefUyTRP7otdO0mFpwEBG50_MCWQg6stTTbpR6c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1327156.RAbgnezefUyTRP7otdO0mFpwEBG50_MCWQg6stTTbpR6c130_provenance.
- NP1327156.RAbgnezefUyTRP7otdO0mFpwEBG50_MCWQg6stTTbpR6c130_assertion description "[Recent work has demonstrated that more than 90% of patients with osteogenesis imperfecta (OI) have mutations in the gene for either the pro alpha 1 (I) chain or the gene for the pro alpha 2 (I) chain of type I procollagen.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327156.RAbgnezefUyTRP7otdO0mFpwEBG50_MCWQg6stTTbpR6c130_provenance.
- NP1327156.RAbgnezefUyTRP7otdO0mFpwEBG50_MCWQg6stTTbpR6c130_assertion evidence source_evidence_literature NP1327156.RAbgnezefUyTRP7otdO0mFpwEBG50_MCWQg6stTTbpR6c130_provenance.
- NP1327156.RAbgnezefUyTRP7otdO0mFpwEBG50_MCWQg6stTTbpR6c130_assertion SIO_000772 7924138 NP1327156.RAbgnezefUyTRP7otdO0mFpwEBG50_MCWQg6stTTbpR6c130_provenance.
- NP1327156.RAbgnezefUyTRP7otdO0mFpwEBG50_MCWQg6stTTbpR6c130_assertion wasDerivedFrom befree-2016 NP1327156.RAbgnezefUyTRP7otdO0mFpwEBG50_MCWQg6stTTbpR6c130_provenance.
- NP1327156.RAbgnezefUyTRP7otdO0mFpwEBG50_MCWQg6stTTbpR6c130_assertion wasGeneratedBy ECO_0000203 NP1327156.RAbgnezefUyTRP7otdO0mFpwEBG50_MCWQg6stTTbpR6c130_provenance.
- befree-2016 importedOn "2016-02-19" NP1327156.RAbgnezefUyTRP7otdO0mFpwEBG50_MCWQg6stTTbpR6c130_provenance.