Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_assertion> ?p ?o ?g. }
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- NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_assertion type Assertion NP885579.RA_SzQqrUzIsCFRlYIq_ppHRl7MiDyxWgRI9NLPL1nDxs130_head.
- 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.