Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_assertion> ?p ?o ?g. }
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- NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_assertion type Assertion NP557081.RA8bLeRYB8eC9NfpMB5sVX0WAbj40dFpjdRFXGRV9QSPk130_head.
- 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.