Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_provenance.
- 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.
- lhgdn-20090331 importedOn "2009-03-31" NP203773.RAP5l4pcrlr5rBWrWS3hjx_LkS32o4bHlKovek16rbk4Q130_provenance.