Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP378119.RA5145AsoI1CXtD9frG_YdmidbNXl1OYG5RcS3ufwTwvs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP378119.RA5145AsoI1CXtD9frG_YdmidbNXl1OYG5RcS3ufwTwvs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP378119.RA5145AsoI1CXtD9frG_YdmidbNXl1OYG5RcS3ufwTwvs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP378119.RA5145AsoI1CXtD9frG_YdmidbNXl1OYG5RcS3ufwTwvs130_provenance.
- NP378119.RA5145AsoI1CXtD9frG_YdmidbNXl1OYG5RcS3ufwTwvs130_assertion description "[Expression of lamin A mutated in the carboxyl-terminal tail generates an aberrant nuclear phenotype similar to that observed in cells from patients with Dunnigan-type partial lipodystrophy and Emery-Dreifuss muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP378119.RA5145AsoI1CXtD9frG_YdmidbNXl1OYG5RcS3ufwTwvs130_provenance.
- NP378119.RA5145AsoI1CXtD9frG_YdmidbNXl1OYG5RcS3ufwTwvs130_assertion evidence source_evidence_literature NP378119.RA5145AsoI1CXtD9frG_YdmidbNXl1OYG5RcS3ufwTwvs130_provenance.
- NP378119.RA5145AsoI1CXtD9frG_YdmidbNXl1OYG5RcS3ufwTwvs130_assertion SIO_000772 12490190 NP378119.RA5145AsoI1CXtD9frG_YdmidbNXl1OYG5RcS3ufwTwvs130_provenance.
- NP378119.RA5145AsoI1CXtD9frG_YdmidbNXl1OYG5RcS3ufwTwvs130_assertion wasDerivedFrom befree-2016 NP378119.RA5145AsoI1CXtD9frG_YdmidbNXl1OYG5RcS3ufwTwvs130_provenance.
- NP378119.RA5145AsoI1CXtD9frG_YdmidbNXl1OYG5RcS3ufwTwvs130_assertion wasGeneratedBy ECO_0000203 NP378119.RA5145AsoI1CXtD9frG_YdmidbNXl1OYG5RcS3ufwTwvs130_provenance.
- befree-2016 importedOn "2016-02-19" NP378119.RA5145AsoI1CXtD9frG_YdmidbNXl1OYG5RcS3ufwTwvs130_provenance.