Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP650896.RAf4b-hkmkIdTnjs6Kb6U4QBYSp9CLLhiX2RvG2QmRGrk130_assertion> ?p ?o ?g. }
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- NP650896.RAf4b-hkmkIdTnjs6Kb6U4QBYSp9CLLhiX2RvG2QmRGrk130_assertion type Assertion NP650896.RAf4b-hkmkIdTnjs6Kb6U4QBYSp9CLLhiX2RvG2QmRGrk130_head.
- NP650896.RAf4b-hkmkIdTnjs6Kb6U4QBYSp9CLLhiX2RvG2QmRGrk130_assertion description "[Mutations in the gene encoding presenilin-1 (PS1) are found in approximately 80% of cases of FAD, with some of these patients presenting cerebellar damage with amyloid plaques and ataxia with unclear pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP650896.RAf4b-hkmkIdTnjs6Kb6U4QBYSp9CLLhiX2RvG2QmRGrk130_provenance.
- NP650896.RAf4b-hkmkIdTnjs6Kb6U4QBYSp9CLLhiX2RvG2QmRGrk130_assertion evidence source_evidence_literature NP650896.RAf4b-hkmkIdTnjs6Kb6U4QBYSp9CLLhiX2RvG2QmRGrk130_provenance.
- NP650896.RAf4b-hkmkIdTnjs6Kb6U4QBYSp9CLLhiX2RvG2QmRGrk130_assertion SIO_000772 24569455 NP650896.RAf4b-hkmkIdTnjs6Kb6U4QBYSp9CLLhiX2RvG2QmRGrk130_provenance.
- NP650896.RAf4b-hkmkIdTnjs6Kb6U4QBYSp9CLLhiX2RvG2QmRGrk130_assertion wasDerivedFrom befree-20150227 NP650896.RAf4b-hkmkIdTnjs6Kb6U4QBYSp9CLLhiX2RvG2QmRGrk130_provenance.
- NP650896.RAf4b-hkmkIdTnjs6Kb6U4QBYSp9CLLhiX2RvG2QmRGrk130_assertion wasGeneratedBy ECO_0000203 NP650896.RAf4b-hkmkIdTnjs6Kb6U4QBYSp9CLLhiX2RvG2QmRGrk130_provenance.