Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_assertion> ?p ?o ?g. }
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- NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_assertion type Assertion NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_head.
- NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_assertion description "[identification of missense mutations in FUS in familial amyotrophic lateral sclerosis type 6; expression studies revealed aberrant localization of mutant FUS protein]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_provenance.
- NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_assertion evidence source_evidence_literature NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_provenance.
- NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_assertion SIO_000772 19251628 NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_provenance.
- NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_assertion wasDerivedFrom lhgdn-20090331 NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_provenance.
- NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_assertion wasGeneratedBy ECO_0000203 NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_provenance.