Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP302236.RAkrRGr9daxOMtEah8Jg43Qkr28sZl0M5T2CYHNdCkXog130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP302236.RAkrRGr9daxOMtEah8Jg43Qkr28sZl0M5T2CYHNdCkXog130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP302236.RAkrRGr9daxOMtEah8Jg43Qkr28sZl0M5T2CYHNdCkXog130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP302236.RAkrRGr9daxOMtEah8Jg43Qkr28sZl0M5T2CYHNdCkXog130_provenance.
- NP302236.RAkrRGr9daxOMtEah8Jg43Qkr28sZl0M5T2CYHNdCkXog130_assertion description "[Frequencies of BcHE K variant, alpha2M insertion and/or deletion polymorphism, the ApoE common polymorphisms and promoter variants at ApoE-491 and -291, were examined by fluorescent RFLP in DNA from 276 United Kingdom Prospective Diabetes Study Type II diabetic subjects and 351 non-diabetic subjects from the Diabetes In Families study.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP302236.RAkrRGr9daxOMtEah8Jg43Qkr28sZl0M5T2CYHNdCkXog130_provenance.
- NP302236.RAkrRGr9daxOMtEah8Jg43Qkr28sZl0M5T2CYHNdCkXog130_assertion evidence source_evidence_literature NP302236.RAkrRGr9daxOMtEah8Jg43Qkr28sZl0M5T2CYHNdCkXog130_provenance.
- NP302236.RAkrRGr9daxOMtEah8Jg43Qkr28sZl0M5T2CYHNdCkXog130_assertion SIO_000772 11793025 NP302236.RAkrRGr9daxOMtEah8Jg43Qkr28sZl0M5T2CYHNdCkXog130_provenance.
- NP302236.RAkrRGr9daxOMtEah8Jg43Qkr28sZl0M5T2CYHNdCkXog130_assertion wasDerivedFrom befree-20140225 NP302236.RAkrRGr9daxOMtEah8Jg43Qkr28sZl0M5T2CYHNdCkXog130_provenance.
- NP302236.RAkrRGr9daxOMtEah8Jg43Qkr28sZl0M5T2CYHNdCkXog130_assertion wasGeneratedBy ECO_0000203 NP302236.RAkrRGr9daxOMtEah8Jg43Qkr28sZl0M5T2CYHNdCkXog130_provenance.
- befree-20140225 importedOn "2014-02-25" NP302236.RAkrRGr9daxOMtEah8Jg43Qkr28sZl0M5T2CYHNdCkXog130_provenance.