Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP710454.RARdVRsIPYVRe3s61IVY6qMDnDoo2qWqBAHgHDFQ6Nx-s130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP710454.RARdVRsIPYVRe3s61IVY6qMDnDoo2qWqBAHgHDFQ6Nx-s130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP710454.RARdVRsIPYVRe3s61IVY6qMDnDoo2qWqBAHgHDFQ6Nx-s130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP710454.RARdVRsIPYVRe3s61IVY6qMDnDoo2qWqBAHgHDFQ6Nx-s130_provenance.
- NP710454.RARdVRsIPYVRe3s61IVY6qMDnDoo2qWqBAHgHDFQ6Nx-s130_assertion description "[Coinheritance of p.R75Q or CF causing CFTR variants with SPINK1 variants significantly increases the risk of ICP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP710454.RARdVRsIPYVRe3s61IVY6qMDnDoo2qWqBAHgHDFQ6Nx-s130_provenance.
- NP710454.RARdVRsIPYVRe3s61IVY6qMDnDoo2qWqBAHgHDFQ6Nx-s130_assertion evidence source_evidence_literature NP710454.RARdVRsIPYVRe3s61IVY6qMDnDoo2qWqBAHgHDFQ6Nx-s130_provenance.
- NP710454.RARdVRsIPYVRe3s61IVY6qMDnDoo2qWqBAHgHDFQ6Nx-s130_assertion SIO_000772 20977904 NP710454.RARdVRsIPYVRe3s61IVY6qMDnDoo2qWqBAHgHDFQ6Nx-s130_provenance.
- NP710454.RARdVRsIPYVRe3s61IVY6qMDnDoo2qWqBAHgHDFQ6Nx-s130_assertion wasDerivedFrom befree-20150227 NP710454.RARdVRsIPYVRe3s61IVY6qMDnDoo2qWqBAHgHDFQ6Nx-s130_provenance.
- NP710454.RARdVRsIPYVRe3s61IVY6qMDnDoo2qWqBAHgHDFQ6Nx-s130_assertion wasGeneratedBy ECO_0000203 NP710454.RARdVRsIPYVRe3s61IVY6qMDnDoo2qWqBAHgHDFQ6Nx-s130_provenance.
- befree-20150227 importedOn "2015-02-27" NP710454.RARdVRsIPYVRe3s61IVY6qMDnDoo2qWqBAHgHDFQ6Nx-s130_provenance.