Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_provenance.
- NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_assertion description "[Rare mutations in LMNA were recently shown to underlie familial partial lipodystrophy (FPLD), a syndrome characterized by regional loss of adipose tissue, insulin resistance, and glucose intolerance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_provenance.
- NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_assertion evidence source_evidence_literature NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_provenance.
- NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_assertion SIO_000772 11243729 NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_provenance.
- NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_assertion wasDerivedFrom befree-20140225 NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_provenance.
- NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_assertion wasGeneratedBy ECO_0000203 NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_provenance.