Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP848159.RA1WI1bjSJVJ7jgS4bBjEuF2nrRCZ0hpGkaqrZZO-cmSU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP848159.RA1WI1bjSJVJ7jgS4bBjEuF2nrRCZ0hpGkaqrZZO-cmSU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP848159.RA1WI1bjSJVJ7jgS4bBjEuF2nrRCZ0hpGkaqrZZO-cmSU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP848159.RA1WI1bjSJVJ7jgS4bBjEuF2nrRCZ0hpGkaqrZZO-cmSU130_provenance.
- NP848159.RA1WI1bjSJVJ7jgS4bBjEuF2nrRCZ0hpGkaqrZZO-cmSU130_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." NP848159.RA1WI1bjSJVJ7jgS4bBjEuF2nrRCZ0hpGkaqrZZO-cmSU130_provenance.
- NP848159.RA1WI1bjSJVJ7jgS4bBjEuF2nrRCZ0hpGkaqrZZO-cmSU130_assertion evidence source_evidence_literature NP848159.RA1WI1bjSJVJ7jgS4bBjEuF2nrRCZ0hpGkaqrZZO-cmSU130_provenance.
- NP848159.RA1WI1bjSJVJ7jgS4bBjEuF2nrRCZ0hpGkaqrZZO-cmSU130_assertion SIO_000772 20977904 NP848159.RA1WI1bjSJVJ7jgS4bBjEuF2nrRCZ0hpGkaqrZZO-cmSU130_provenance.
- NP848159.RA1WI1bjSJVJ7jgS4bBjEuF2nrRCZ0hpGkaqrZZO-cmSU130_assertion wasDerivedFrom befree-2016 NP848159.RA1WI1bjSJVJ7jgS4bBjEuF2nrRCZ0hpGkaqrZZO-cmSU130_provenance.
- NP848159.RA1WI1bjSJVJ7jgS4bBjEuF2nrRCZ0hpGkaqrZZO-cmSU130_assertion wasGeneratedBy ECO_0000203 NP848159.RA1WI1bjSJVJ7jgS4bBjEuF2nrRCZ0hpGkaqrZZO-cmSU130_provenance.
- befree-2016 importedOn "2016-02-19" NP848159.RA1WI1bjSJVJ7jgS4bBjEuF2nrRCZ0hpGkaqrZZO-cmSU130_provenance.