Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP145032.RAiMuF60V9PaWWOVXpwtNtaJY98H4wFHbkWQc9ZDrc1oA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP145032.RAiMuF60V9PaWWOVXpwtNtaJY98H4wFHbkWQc9ZDrc1oA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP145032.RAiMuF60V9PaWWOVXpwtNtaJY98H4wFHbkWQc9ZDrc1oA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP145032.RAiMuF60V9PaWWOVXpwtNtaJY98H4wFHbkWQc9ZDrc1oA130_provenance.
- NP145032.RAiMuF60V9PaWWOVXpwtNtaJY98H4wFHbkWQc9ZDrc1oA130_assertion description "[Congenital lipodystrophy patients with Seipin mutations have a more severe lack of body fat, which affects both metabolically active and mechanical adipose tissue, compared with patients with mutations in the AGPAT2 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP145032.RAiMuF60V9PaWWOVXpwtNtaJY98H4wFHbkWQc9ZDrc1oA130_provenance.
- NP145032.RAiMuF60V9PaWWOVXpwtNtaJY98H4wFHbkWQc9ZDrc1oA130_assertion evidence source_evidence_literature NP145032.RAiMuF60V9PaWWOVXpwtNtaJY98H4wFHbkWQc9ZDrc1oA130_provenance.
- NP145032.RAiMuF60V9PaWWOVXpwtNtaJY98H4wFHbkWQc9ZDrc1oA130_assertion SIO_000772 14602785 NP145032.RAiMuF60V9PaWWOVXpwtNtaJY98H4wFHbkWQc9ZDrc1oA130_provenance.
- NP145032.RAiMuF60V9PaWWOVXpwtNtaJY98H4wFHbkWQc9ZDrc1oA130_assertion wasDerivedFrom lhgdn-20090331 NP145032.RAiMuF60V9PaWWOVXpwtNtaJY98H4wFHbkWQc9ZDrc1oA130_provenance.
- NP145032.RAiMuF60V9PaWWOVXpwtNtaJY98H4wFHbkWQc9ZDrc1oA130_assertion wasGeneratedBy ECO_0000203 NP145032.RAiMuF60V9PaWWOVXpwtNtaJY98H4wFHbkWQc9ZDrc1oA130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP145032.RAiMuF60V9PaWWOVXpwtNtaJY98H4wFHbkWQc9ZDrc1oA130_provenance.