Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP760928.RAO0X00h2au-wRaZG0oOlVfNT7iPrRsKQAYNBn44PAJlk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP760928.RAO0X00h2au-wRaZG0oOlVfNT7iPrRsKQAYNBn44PAJlk130_assertion type Assertion NP760928.RAO0X00h2au-wRaZG0oOlVfNT7iPrRsKQAYNBn44PAJlk130_head.
- NP760928.RAO0X00h2au-wRaZG0oOlVfNT7iPrRsKQAYNBn44PAJlk130_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." NP760928.RAO0X00h2au-wRaZG0oOlVfNT7iPrRsKQAYNBn44PAJlk130_provenance.
- NP760928.RAO0X00h2au-wRaZG0oOlVfNT7iPrRsKQAYNBn44PAJlk130_assertion evidence source_evidence_literature NP760928.RAO0X00h2au-wRaZG0oOlVfNT7iPrRsKQAYNBn44PAJlk130_provenance.
- NP760928.RAO0X00h2au-wRaZG0oOlVfNT7iPrRsKQAYNBn44PAJlk130_assertion SIO_000772 10556190 NP760928.RAO0X00h2au-wRaZG0oOlVfNT7iPrRsKQAYNBn44PAJlk130_provenance.
- NP760928.RAO0X00h2au-wRaZG0oOlVfNT7iPrRsKQAYNBn44PAJlk130_assertion wasDerivedFrom befree-20140225 NP760928.RAO0X00h2au-wRaZG0oOlVfNT7iPrRsKQAYNBn44PAJlk130_provenance.
- NP760928.RAO0X00h2au-wRaZG0oOlVfNT7iPrRsKQAYNBn44PAJlk130_assertion wasGeneratedBy ECO_0000203 NP760928.RAO0X00h2au-wRaZG0oOlVfNT7iPrRsKQAYNBn44PAJlk130_provenance.