Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_provenance.
- NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_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." NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_provenance.
- NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_assertion evidence source_evidence_literature NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_provenance.
- NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_assertion SIO_000772 20977904 NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_provenance.
- NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_assertion wasDerivedFrom befree-20140225 NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_provenance.
- NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_assertion wasGeneratedBy ECO_0000203 NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_provenance.