Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP616738.RAgwohczKsOWuNCEudUS4xUOpmmYuHpb5yGRDQCcm3ITU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP616738.RAgwohczKsOWuNCEudUS4xUOpmmYuHpb5yGRDQCcm3ITU130_assertion type Assertion NP616738.RAgwohczKsOWuNCEudUS4xUOpmmYuHpb5yGRDQCcm3ITU130_head.
- NP616738.RAgwohczKsOWuNCEudUS4xUOpmmYuHpb5yGRDQCcm3ITU130_assertion description "[Mutations in the PFN1 gene are not a common cause in patients with amyotrophic lateral sclerosis and frontotemporal lobar degeneration in France.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP616738.RAgwohczKsOWuNCEudUS4xUOpmmYuHpb5yGRDQCcm3ITU130_provenance.
- NP616738.RAgwohczKsOWuNCEudUS4xUOpmmYuHpb5yGRDQCcm3ITU130_assertion evidence source_evidence_literature NP616738.RAgwohczKsOWuNCEudUS4xUOpmmYuHpb5yGRDQCcm3ITU130_provenance.
- NP616738.RAgwohczKsOWuNCEudUS4xUOpmmYuHpb5yGRDQCcm3ITU130_assertion SIO_000772 23182804 NP616738.RAgwohczKsOWuNCEudUS4xUOpmmYuHpb5yGRDQCcm3ITU130_provenance.
- NP616738.RAgwohczKsOWuNCEudUS4xUOpmmYuHpb5yGRDQCcm3ITU130_assertion wasDerivedFrom befree-20150227 NP616738.RAgwohczKsOWuNCEudUS4xUOpmmYuHpb5yGRDQCcm3ITU130_provenance.
- NP616738.RAgwohczKsOWuNCEudUS4xUOpmmYuHpb5yGRDQCcm3ITU130_assertion wasGeneratedBy ECO_0000203 NP616738.RAgwohczKsOWuNCEudUS4xUOpmmYuHpb5yGRDQCcm3ITU130_provenance.