Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP574774.RACvv-KitywXIr81zK76DzZj3GJabi_wtD18GXOZwxZIE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP574774.RACvv-KitywXIr81zK76DzZj3GJabi_wtD18GXOZwxZIE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP574774.RACvv-KitywXIr81zK76DzZj3GJabi_wtD18GXOZwxZIE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP574774.RACvv-KitywXIr81zK76DzZj3GJabi_wtD18GXOZwxZIE130_provenance.
- NP574774.RACvv-KitywXIr81zK76DzZj3GJabi_wtD18GXOZwxZIE130_assertion description "[Screening for C677T and A1298C MTHFR polymorphisms in patients with epilepsy and risk of hyperhomocysteinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP574774.RACvv-KitywXIr81zK76DzZj3GJabi_wtD18GXOZwxZIE130_provenance.
- NP574774.RACvv-KitywXIr81zK76DzZj3GJabi_wtD18GXOZwxZIE130_assertion evidence source_evidence_literature NP574774.RACvv-KitywXIr81zK76DzZj3GJabi_wtD18GXOZwxZIE130_provenance.
- NP574774.RACvv-KitywXIr81zK76DzZj3GJabi_wtD18GXOZwxZIE130_assertion SIO_000772 15970629 NP574774.RACvv-KitywXIr81zK76DzZj3GJabi_wtD18GXOZwxZIE130_provenance.
- NP574774.RACvv-KitywXIr81zK76DzZj3GJabi_wtD18GXOZwxZIE130_assertion wasDerivedFrom befree-20150227 NP574774.RACvv-KitywXIr81zK76DzZj3GJabi_wtD18GXOZwxZIE130_provenance.
- NP574774.RACvv-KitywXIr81zK76DzZj3GJabi_wtD18GXOZwxZIE130_assertion wasGeneratedBy ECO_0000203 NP574774.RACvv-KitywXIr81zK76DzZj3GJabi_wtD18GXOZwxZIE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP574774.RACvv-KitywXIr81zK76DzZj3GJabi_wtD18GXOZwxZIE130_provenance.