Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP42536.RAiy1gtC07mzrL7rVLv_sQsw54DohrIdKM78J1WEO6wK0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP42536.RAiy1gtC07mzrL7rVLv_sQsw54DohrIdKM78J1WEO6wK0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP42536.RAiy1gtC07mzrL7rVLv_sQsw54DohrIdKM78J1WEO6wK0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP42536.RAiy1gtC07mzrL7rVLv_sQsw54DohrIdKM78J1WEO6wK0130_provenance.
- NP42536.RAiy1gtC07mzrL7rVLv_sQsw54DohrIdKM78J1WEO6wK0130_assertion description "[We conclude that mutations of the HKII gene are not a major etiological factor for NIDDM in the Finnish population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP42536.RAiy1gtC07mzrL7rVLv_sQsw54DohrIdKM78J1WEO6wK0130_provenance.
- NP42536.RAiy1gtC07mzrL7rVLv_sQsw54DohrIdKM78J1WEO6wK0130_assertion evidence source_evidence_literature NP42536.RAiy1gtC07mzrL7rVLv_sQsw54DohrIdKM78J1WEO6wK0130_provenance.
- NP42536.RAiy1gtC07mzrL7rVLv_sQsw54DohrIdKM78J1WEO6wK0130_assertion SIO_000772 7883120 NP42536.RAiy1gtC07mzrL7rVLv_sQsw54DohrIdKM78J1WEO6wK0130_provenance.
- NP42536.RAiy1gtC07mzrL7rVLv_sQsw54DohrIdKM78J1WEO6wK0130_assertion wasDerivedFrom gad-20130706 NP42536.RAiy1gtC07mzrL7rVLv_sQsw54DohrIdKM78J1WEO6wK0130_provenance.
- NP42536.RAiy1gtC07mzrL7rVLv_sQsw54DohrIdKM78J1WEO6wK0130_assertion wasGeneratedBy ECO_0000203 NP42536.RAiy1gtC07mzrL7rVLv_sQsw54DohrIdKM78J1WEO6wK0130_provenance.
- gad-20130706 importedOn "2013-07-06" NP42536.RAiy1gtC07mzrL7rVLv_sQsw54DohrIdKM78J1WEO6wK0130_provenance.