Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_assertion> ?p ?o ?g. }
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- NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_assertion type Assertion NP513712.RAdVw2Lcr71gt2bNFBB2k5uBZGetEdQzlw2TM-ou1UmPk130_head.
- 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.