Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP786457.RAi94lRYnw67YtSHcdE85KmpyrtnyTWsQMAzQXNSTocz8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP786457.RAi94lRYnw67YtSHcdE85KmpyrtnyTWsQMAzQXNSTocz8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP786457.RAi94lRYnw67YtSHcdE85KmpyrtnyTWsQMAzQXNSTocz8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP786457.RAi94lRYnw67YtSHcdE85KmpyrtnyTWsQMAzQXNSTocz8130_provenance.
- NP786457.RAi94lRYnw67YtSHcdE85KmpyrtnyTWsQMAzQXNSTocz8130_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." NP786457.RAi94lRYnw67YtSHcdE85KmpyrtnyTWsQMAzQXNSTocz8130_provenance.
- NP786457.RAi94lRYnw67YtSHcdE85KmpyrtnyTWsQMAzQXNSTocz8130_assertion evidence source_evidence_literature NP786457.RAi94lRYnw67YtSHcdE85KmpyrtnyTWsQMAzQXNSTocz8130_provenance.
- NP786457.RAi94lRYnw67YtSHcdE85KmpyrtnyTWsQMAzQXNSTocz8130_assertion SIO_000772 20977904 NP786457.RAi94lRYnw67YtSHcdE85KmpyrtnyTWsQMAzQXNSTocz8130_provenance.
- NP786457.RAi94lRYnw67YtSHcdE85KmpyrtnyTWsQMAzQXNSTocz8130_assertion wasDerivedFrom befree-20140225 NP786457.RAi94lRYnw67YtSHcdE85KmpyrtnyTWsQMAzQXNSTocz8130_provenance.
- NP786457.RAi94lRYnw67YtSHcdE85KmpyrtnyTWsQMAzQXNSTocz8130_assertion wasGeneratedBy ECO_0000203 NP786457.RAi94lRYnw67YtSHcdE85KmpyrtnyTWsQMAzQXNSTocz8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP786457.RAi94lRYnw67YtSHcdE85KmpyrtnyTWsQMAzQXNSTocz8130_provenance.