Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_provenance.
- NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_assertion description "[Missense mutations in MIP underlie autosomal dominant 'polymorphic' and lamellar cataracts linked to 12q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_provenance.
- NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_assertion evidence source_evidence_literature NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_provenance.
- NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_assertion SIO_000772 10802646 NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_provenance.
- NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_assertion wasDerivedFrom befree-20150227 NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_provenance.
- NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_assertion wasGeneratedBy ECO_0000203 NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP1009131.RAnRWjdS2TNGuyiM5CkgCKW4QhkOhHWUFupV8Fe0nLvMo130_provenance.