Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1399101.RAGXXx0-sQvz4MybmLEHUGQuY071iQYeQ8PakBV3SmDCY130_assertion> ?p ?o ?g. }
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- NP1399101.RAGXXx0-sQvz4MybmLEHUGQuY071iQYeQ8PakBV3SmDCY130_assertion type Assertion NP1399101.RAGXXx0-sQvz4MybmLEHUGQuY071iQYeQ8PakBV3SmDCY130_head.
- NP1399101.RAGXXx0-sQvz4MybmLEHUGQuY071iQYeQ8PakBV3SmDCY130_assertion description "[These patients were genotyped for vascular disease-associated polymorphisms in the genes coding for methylenetetrahydrofolate reductase (MTHFR), angiotensin-converting enzyme (ACE), factor V Leiden (FVL), and a common genetic risk factor for AD, apolipoprotein E epsilon4 (APOE epsilon4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1399101.RAGXXx0-sQvz4MybmLEHUGQuY071iQYeQ8PakBV3SmDCY130_provenance.
- NP1399101.RAGXXx0-sQvz4MybmLEHUGQuY071iQYeQ8PakBV3SmDCY130_assertion evidence source_evidence_literature NP1399101.RAGXXx0-sQvz4MybmLEHUGQuY071iQYeQ8PakBV3SmDCY130_provenance.
- NP1399101.RAGXXx0-sQvz4MybmLEHUGQuY071iQYeQ8PakBV3SmDCY130_assertion SIO_000772 9660395 NP1399101.RAGXXx0-sQvz4MybmLEHUGQuY071iQYeQ8PakBV3SmDCY130_provenance.
- NP1399101.RAGXXx0-sQvz4MybmLEHUGQuY071iQYeQ8PakBV3SmDCY130_assertion wasDerivedFrom befree-2016 NP1399101.RAGXXx0-sQvz4MybmLEHUGQuY071iQYeQ8PakBV3SmDCY130_provenance.
- NP1399101.RAGXXx0-sQvz4MybmLEHUGQuY071iQYeQ8PakBV3SmDCY130_assertion wasGeneratedBy ECO_0000203 NP1399101.RAGXXx0-sQvz4MybmLEHUGQuY071iQYeQ8PakBV3SmDCY130_provenance.