Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP208545.RAAY9gIzdaZS1lvZ6q5c37Br922bcCOAEEVUPNFm-dpIk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP208545.RAAY9gIzdaZS1lvZ6q5c37Br922bcCOAEEVUPNFm-dpIk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP208545.RAAY9gIzdaZS1lvZ6q5c37Br922bcCOAEEVUPNFm-dpIk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP208545.RAAY9gIzdaZS1lvZ6q5c37Br922bcCOAEEVUPNFm-dpIk130_provenance.
- NP208545.RAAY9gIzdaZS1lvZ6q5c37Br922bcCOAEEVUPNFm-dpIk130_assertion description "[The lamin A/C (LMNA) gene, mutations of which cause rare syndromes of severe insulin resistance and dyslipidemia, is located on chromosome 1q21-q24, a region linked to T2DM in several genome wide scans, including in the Old Order Amish.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208545.RAAY9gIzdaZS1lvZ6q5c37Br922bcCOAEEVUPNFm-dpIk130_provenance.
- NP208545.RAAY9gIzdaZS1lvZ6q5c37Br922bcCOAEEVUPNFm-dpIk130_assertion evidence source_evidence_literature NP208545.RAAY9gIzdaZS1lvZ6q5c37Br922bcCOAEEVUPNFm-dpIk130_provenance.
- NP208545.RAAY9gIzdaZS1lvZ6q5c37Br922bcCOAEEVUPNFm-dpIk130_assertion SIO_000772 15205219 NP208545.RAAY9gIzdaZS1lvZ6q5c37Br922bcCOAEEVUPNFm-dpIk130_provenance.
- NP208545.RAAY9gIzdaZS1lvZ6q5c37Br922bcCOAEEVUPNFm-dpIk130_assertion wasDerivedFrom befree-20140225 NP208545.RAAY9gIzdaZS1lvZ6q5c37Br922bcCOAEEVUPNFm-dpIk130_provenance.
- NP208545.RAAY9gIzdaZS1lvZ6q5c37Br922bcCOAEEVUPNFm-dpIk130_assertion wasGeneratedBy ECO_0000203 NP208545.RAAY9gIzdaZS1lvZ6q5c37Br922bcCOAEEVUPNFm-dpIk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP208545.RAAY9gIzdaZS1lvZ6q5c37Br922bcCOAEEVUPNFm-dpIk130_provenance.