Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP304706.RAWnsiUkv1pvz8F-7STU4NeHUE79EpMYk5gA7l8krwQDU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP304706.RAWnsiUkv1pvz8F-7STU4NeHUE79EpMYk5gA7l8krwQDU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP304706.RAWnsiUkv1pvz8F-7STU4NeHUE79EpMYk5gA7l8krwQDU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP304706.RAWnsiUkv1pvz8F-7STU4NeHUE79EpMYk5gA7l8krwQDU130_provenance.
- NP304706.RAWnsiUkv1pvz8F-7STU4NeHUE79EpMYk5gA7l8krwQDU130_assertion description "[We used the following four candidate gene polymorphisms: angiotensin converting enzyme (ACE)/Insertion(I)-Deletion(D), angiotensinogen (AGT)/M235T, angiotensin II type 1 receptor (AT1)/ A1166C, type 2 receptor (AT2)/C3123A, to examine the association between polymorphisms and the severity of lacunar infarction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP304706.RAWnsiUkv1pvz8F-7STU4NeHUE79EpMYk5gA7l8krwQDU130_provenance.
- NP304706.RAWnsiUkv1pvz8F-7STU4NeHUE79EpMYk5gA7l8krwQDU130_assertion evidence source_evidence_literature NP304706.RAWnsiUkv1pvz8F-7STU4NeHUE79EpMYk5gA7l8krwQDU130_provenance.
- NP304706.RAWnsiUkv1pvz8F-7STU4NeHUE79EpMYk5gA7l8krwQDU130_assertion SIO_000772 10701810 NP304706.RAWnsiUkv1pvz8F-7STU4NeHUE79EpMYk5gA7l8krwQDU130_provenance.
- NP304706.RAWnsiUkv1pvz8F-7STU4NeHUE79EpMYk5gA7l8krwQDU130_assertion wasDerivedFrom befree-20140225 NP304706.RAWnsiUkv1pvz8F-7STU4NeHUE79EpMYk5gA7l8krwQDU130_provenance.
- NP304706.RAWnsiUkv1pvz8F-7STU4NeHUE79EpMYk5gA7l8krwQDU130_assertion wasGeneratedBy ECO_0000203 NP304706.RAWnsiUkv1pvz8F-7STU4NeHUE79EpMYk5gA7l8krwQDU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP304706.RAWnsiUkv1pvz8F-7STU4NeHUE79EpMYk5gA7l8krwQDU130_provenance.