Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP574557.RAK9alY8sYugh2CTKbzB1dlLmDm0kcs9qVlWZgwELtUpg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP574557.RAK9alY8sYugh2CTKbzB1dlLmDm0kcs9qVlWZgwELtUpg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP574557.RAK9alY8sYugh2CTKbzB1dlLmDm0kcs9qVlWZgwELtUpg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP574557.RAK9alY8sYugh2CTKbzB1dlLmDm0kcs9qVlWZgwELtUpg130_provenance.
- NP574557.RAK9alY8sYugh2CTKbzB1dlLmDm0kcs9qVlWZgwELtUpg130_assertion description "[The preliminary results obtained in this study revealed an association of the MTHFR and APOE gene polymorphism with cerebrovascular disease, suggesting a significant risk for stroke in subjects who are homozygous for the T allele and for carotid stenosis in subjects having APOEepsilon3epsilon4 genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP574557.RAK9alY8sYugh2CTKbzB1dlLmDm0kcs9qVlWZgwELtUpg130_provenance.
- NP574557.RAK9alY8sYugh2CTKbzB1dlLmDm0kcs9qVlWZgwELtUpg130_assertion evidence source_evidence_literature NP574557.RAK9alY8sYugh2CTKbzB1dlLmDm0kcs9qVlWZgwELtUpg130_provenance.
- NP574557.RAK9alY8sYugh2CTKbzB1dlLmDm0kcs9qVlWZgwELtUpg130_assertion SIO_000772 11388660 NP574557.RAK9alY8sYugh2CTKbzB1dlLmDm0kcs9qVlWZgwELtUpg130_provenance.
- NP574557.RAK9alY8sYugh2CTKbzB1dlLmDm0kcs9qVlWZgwELtUpg130_assertion wasDerivedFrom befree-20150227 NP574557.RAK9alY8sYugh2CTKbzB1dlLmDm0kcs9qVlWZgwELtUpg130_provenance.
- NP574557.RAK9alY8sYugh2CTKbzB1dlLmDm0kcs9qVlWZgwELtUpg130_assertion wasGeneratedBy ECO_0000203 NP574557.RAK9alY8sYugh2CTKbzB1dlLmDm0kcs9qVlWZgwELtUpg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP574557.RAK9alY8sYugh2CTKbzB1dlLmDm0kcs9qVlWZgwELtUpg130_provenance.