Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP595127.RA3_sQENk0EJsEmWqTKv7fHtH5_ID_adT7dxn1MZomvoI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP595127.RA3_sQENk0EJsEmWqTKv7fHtH5_ID_adT7dxn1MZomvoI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP595127.RA3_sQENk0EJsEmWqTKv7fHtH5_ID_adT7dxn1MZomvoI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP595127.RA3_sQENk0EJsEmWqTKv7fHtH5_ID_adT7dxn1MZomvoI130_provenance.
- NP595127.RA3_sQENk0EJsEmWqTKv7fHtH5_ID_adT7dxn1MZomvoI130_assertion description "[We previously identified mutations in the Lpin1 gene, encoding lipin-1, as the underlying cause of lipodystrophy in the fatty liver dystrophy (fld) mutant mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP595127.RA3_sQENk0EJsEmWqTKv7fHtH5_ID_adT7dxn1MZomvoI130_provenance.
- NP595127.RA3_sQENk0EJsEmWqTKv7fHtH5_ID_adT7dxn1MZomvoI130_assertion evidence source_evidence_literature NP595127.RA3_sQENk0EJsEmWqTKv7fHtH5_ID_adT7dxn1MZomvoI130_provenance.
- NP595127.RA3_sQENk0EJsEmWqTKv7fHtH5_ID_adT7dxn1MZomvoI130_assertion SIO_000772 17158099 NP595127.RA3_sQENk0EJsEmWqTKv7fHtH5_ID_adT7dxn1MZomvoI130_provenance.
- NP595127.RA3_sQENk0EJsEmWqTKv7fHtH5_ID_adT7dxn1MZomvoI130_assertion wasDerivedFrom befree-20140225 NP595127.RA3_sQENk0EJsEmWqTKv7fHtH5_ID_adT7dxn1MZomvoI130_provenance.
- NP595127.RA3_sQENk0EJsEmWqTKv7fHtH5_ID_adT7dxn1MZomvoI130_assertion wasGeneratedBy ECO_0000203 NP595127.RA3_sQENk0EJsEmWqTKv7fHtH5_ID_adT7dxn1MZomvoI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP595127.RA3_sQENk0EJsEmWqTKv7fHtH5_ID_adT7dxn1MZomvoI130_provenance.