Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP443912.RAfifLr-WCg44UiSRE3J-bP3bfxT8WMfJSZi7bZhwzs8M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP443912.RAfifLr-WCg44UiSRE3J-bP3bfxT8WMfJSZi7bZhwzs8M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP443912.RAfifLr-WCg44UiSRE3J-bP3bfxT8WMfJSZi7bZhwzs8M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP443912.RAfifLr-WCg44UiSRE3J-bP3bfxT8WMfJSZi7bZhwzs8M130_provenance.
- NP443912.RAfifLr-WCg44UiSRE3J-bP3bfxT8WMfJSZi7bZhwzs8M130_assertion description "[Furthermore, we examined genetic variations in glucose-6-phosphate dehydrogenase (G6PD) and HBA (?-globin) genes to determine their association with intracranial vasculopathy in children with SCA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP443912.RAfifLr-WCg44UiSRE3J-bP3bfxT8WMfJSZi7bZhwzs8M130_provenance.
- NP443912.RAfifLr-WCg44UiSRE3J-bP3bfxT8WMfJSZi7bZhwzs8M130_assertion evidence source_evidence_literature NP443912.RAfifLr-WCg44UiSRE3J-bP3bfxT8WMfJSZi7bZhwzs8M130_provenance.
- NP443912.RAfifLr-WCg44UiSRE3J-bP3bfxT8WMfJSZi7bZhwzs8M130_assertion SIO_000772 22958163 NP443912.RAfifLr-WCg44UiSRE3J-bP3bfxT8WMfJSZi7bZhwzs8M130_provenance.
- NP443912.RAfifLr-WCg44UiSRE3J-bP3bfxT8WMfJSZi7bZhwzs8M130_assertion wasDerivedFrom befree-20150227 NP443912.RAfifLr-WCg44UiSRE3J-bP3bfxT8WMfJSZi7bZhwzs8M130_provenance.
- NP443912.RAfifLr-WCg44UiSRE3J-bP3bfxT8WMfJSZi7bZhwzs8M130_assertion wasGeneratedBy ECO_0000203 NP443912.RAfifLr-WCg44UiSRE3J-bP3bfxT8WMfJSZi7bZhwzs8M130_provenance.
- befree-20150227 importedOn "2015-02-27" NP443912.RAfifLr-WCg44UiSRE3J-bP3bfxT8WMfJSZi7bZhwzs8M130_provenance.