Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP937290.RAqLs_W2ZARM987bp1hV56J7iaabfmhSnlnKfAr2pVMsM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP937290.RAqLs_W2ZARM987bp1hV56J7iaabfmhSnlnKfAr2pVMsM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP937290.RAqLs_W2ZARM987bp1hV56J7iaabfmhSnlnKfAr2pVMsM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP937290.RAqLs_W2ZARM987bp1hV56J7iaabfmhSnlnKfAr2pVMsM130_provenance.
- NP937290.RAqLs_W2ZARM987bp1hV56J7iaabfmhSnlnKfAr2pVMsM130_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." NP937290.RAqLs_W2ZARM987bp1hV56J7iaabfmhSnlnKfAr2pVMsM130_provenance.
- NP937290.RAqLs_W2ZARM987bp1hV56J7iaabfmhSnlnKfAr2pVMsM130_assertion evidence source_evidence_literature NP937290.RAqLs_W2ZARM987bp1hV56J7iaabfmhSnlnKfAr2pVMsM130_provenance.
- NP937290.RAqLs_W2ZARM987bp1hV56J7iaabfmhSnlnKfAr2pVMsM130_assertion SIO_000772 10802646 NP937290.RAqLs_W2ZARM987bp1hV56J7iaabfmhSnlnKfAr2pVMsM130_provenance.
- NP937290.RAqLs_W2ZARM987bp1hV56J7iaabfmhSnlnKfAr2pVMsM130_assertion wasDerivedFrom befree-20140225 NP937290.RAqLs_W2ZARM987bp1hV56J7iaabfmhSnlnKfAr2pVMsM130_provenance.
- NP937290.RAqLs_W2ZARM987bp1hV56J7iaabfmhSnlnKfAr2pVMsM130_assertion wasGeneratedBy ECO_0000203 NP937290.RAqLs_W2ZARM987bp1hV56J7iaabfmhSnlnKfAr2pVMsM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP937290.RAqLs_W2ZARM987bp1hV56J7iaabfmhSnlnKfAr2pVMsM130_provenance.