Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP537382.RA29uKGsdno6AJVc8JUcHqDFhoLBIaWTdhXC2pUnZF_iw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP537382.RA29uKGsdno6AJVc8JUcHqDFhoLBIaWTdhXC2pUnZF_iw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP537382.RA29uKGsdno6AJVc8JUcHqDFhoLBIaWTdhXC2pUnZF_iw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP537382.RA29uKGsdno6AJVc8JUcHqDFhoLBIaWTdhXC2pUnZF_iw130_provenance.
- NP537382.RA29uKGsdno6AJVc8JUcHqDFhoLBIaWTdhXC2pUnZF_iw130_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." NP537382.RA29uKGsdno6AJVc8JUcHqDFhoLBIaWTdhXC2pUnZF_iw130_provenance.
- NP537382.RA29uKGsdno6AJVc8JUcHqDFhoLBIaWTdhXC2pUnZF_iw130_assertion evidence source_evidence_literature NP537382.RA29uKGsdno6AJVc8JUcHqDFhoLBIaWTdhXC2pUnZF_iw130_provenance.
- NP537382.RA29uKGsdno6AJVc8JUcHqDFhoLBIaWTdhXC2pUnZF_iw130_assertion SIO_000772 15205219 NP537382.RA29uKGsdno6AJVc8JUcHqDFhoLBIaWTdhXC2pUnZF_iw130_provenance.
- NP537382.RA29uKGsdno6AJVc8JUcHqDFhoLBIaWTdhXC2pUnZF_iw130_assertion wasDerivedFrom befree-20150227 NP537382.RA29uKGsdno6AJVc8JUcHqDFhoLBIaWTdhXC2pUnZF_iw130_provenance.
- NP537382.RA29uKGsdno6AJVc8JUcHqDFhoLBIaWTdhXC2pUnZF_iw130_assertion wasGeneratedBy ECO_0000203 NP537382.RA29uKGsdno6AJVc8JUcHqDFhoLBIaWTdhXC2pUnZF_iw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP537382.RA29uKGsdno6AJVc8JUcHqDFhoLBIaWTdhXC2pUnZF_iw130_provenance.