Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP472507.RAlMhrXPW91HJ-nJib8dk1gsnpBxM1BYDQAIoz-qlX96g130_assertion> ?p ?o ?g. }
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- NP472507.RAlMhrXPW91HJ-nJib8dk1gsnpBxM1BYDQAIoz-qlX96g130_assertion type Assertion NP472507.RAlMhrXPW91HJ-nJib8dk1gsnpBxM1BYDQAIoz-qlX96g130_head.
- NP472507.RAlMhrXPW91HJ-nJib8dk1gsnpBxM1BYDQAIoz-qlX96g130_assertion description "[With the aim of establishing whether the HR2 haplotype in factor V affects the risk of venous thromboembolism, a retrospective multicenter cohort study was performed in 810 family members identified through 174 probands who suffered from at least 1 episode of deep vein thrombosis and/or pulmonary embolism and had an inherited defect associated with thrombophilia (antithrombin, protein C, or protein S deficiency; factor V R506Q or prothrombin G20210A).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP472507.RAlMhrXPW91HJ-nJib8dk1gsnpBxM1BYDQAIoz-qlX96g130_provenance.
- NP472507.RAlMhrXPW91HJ-nJib8dk1gsnpBxM1BYDQAIoz-qlX96g130_assertion evidence source_evidence_literature NP472507.RAlMhrXPW91HJ-nJib8dk1gsnpBxM1BYDQAIoz-qlX96g130_provenance.
- NP472507.RAlMhrXPW91HJ-nJib8dk1gsnpBxM1BYDQAIoz-qlX96g130_assertion SIO_000772 10556190 NP472507.RAlMhrXPW91HJ-nJib8dk1gsnpBxM1BYDQAIoz-qlX96g130_provenance.
- NP472507.RAlMhrXPW91HJ-nJib8dk1gsnpBxM1BYDQAIoz-qlX96g130_assertion wasDerivedFrom befree-20140225 NP472507.RAlMhrXPW91HJ-nJib8dk1gsnpBxM1BYDQAIoz-qlX96g130_provenance.
- NP472507.RAlMhrXPW91HJ-nJib8dk1gsnpBxM1BYDQAIoz-qlX96g130_assertion wasGeneratedBy ECO_0000203 NP472507.RAlMhrXPW91HJ-nJib8dk1gsnpBxM1BYDQAIoz-qlX96g130_provenance.