Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_provenance.
- NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_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." NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_provenance.
- NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_assertion evidence source_evidence_literature NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_provenance.
- NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_assertion SIO_000772 10802646 NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_provenance.
- NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_assertion wasDerivedFrom befree-20150227 NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_provenance.
- NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_assertion wasGeneratedBy ECO_0000203 NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_provenance.