Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_provenance.
- NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_assertion description "[Mutations in the cohesin regulators NIPBL and ESCO2 are causative of the Cornelia de Lange syndrome (CdLS) and Roberts or SC phocomelia syndrome, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_provenance.
- NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_assertion evidence source_evidence_literature NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_provenance.
- NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_assertion SIO_000772 17273969 NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_provenance.
- NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_assertion wasDerivedFrom befree-20140225 NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_provenance.
- NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_assertion wasGeneratedBy ECO_0000203 NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP477820.RARqqnihpw_otm4RoYD-R0WoCOiMWcBN0Ndu5XCUVr1sg130_provenance.