Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP168854.RADzHC5RoNrTrUc13T8EkQgF-QmpXK46_RZvS5WtvSoSQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP168854.RADzHC5RoNrTrUc13T8EkQgF-QmpXK46_RZvS5WtvSoSQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP168854.RADzHC5RoNrTrUc13T8EkQgF-QmpXK46_RZvS5WtvSoSQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP168854.RADzHC5RoNrTrUc13T8EkQgF-QmpXK46_RZvS5WtvSoSQ130_provenance.
- NP168854.RADzHC5RoNrTrUc13T8EkQgF-QmpXK46_RZvS5WtvSoSQ130_assertion description "[Autosomal dominant familial partial lipodystrophy (FPLD) due to mutant LMNA encoding nuclear lamin A/C is characterized by adipose tissue repartitioning together with multiple metabolic disturbances, including insulin resistance and dyslipidemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP168854.RADzHC5RoNrTrUc13T8EkQgF-QmpXK46_RZvS5WtvSoSQ130_provenance.
- NP168854.RADzHC5RoNrTrUc13T8EkQgF-QmpXK46_RZvS5WtvSoSQ130_assertion evidence source_evidence_literature NP168854.RADzHC5RoNrTrUc13T8EkQgF-QmpXK46_RZvS5WtvSoSQ130_provenance.
- NP168854.RADzHC5RoNrTrUc13T8EkQgF-QmpXK46_RZvS5WtvSoSQ130_assertion SIO_000772 12453919 NP168854.RADzHC5RoNrTrUc13T8EkQgF-QmpXK46_RZvS5WtvSoSQ130_provenance.
- NP168854.RADzHC5RoNrTrUc13T8EkQgF-QmpXK46_RZvS5WtvSoSQ130_assertion wasDerivedFrom befree-20140225 NP168854.RADzHC5RoNrTrUc13T8EkQgF-QmpXK46_RZvS5WtvSoSQ130_provenance.
- NP168854.RADzHC5RoNrTrUc13T8EkQgF-QmpXK46_RZvS5WtvSoSQ130_assertion wasGeneratedBy ECO_0000203 NP168854.RADzHC5RoNrTrUc13T8EkQgF-QmpXK46_RZvS5WtvSoSQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP168854.RADzHC5RoNrTrUc13T8EkQgF-QmpXK46_RZvS5WtvSoSQ130_provenance.