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- source_evidence_literature type ECO_0000212 NP917613.RARI4DwCAdMZ3nrMY6SKK8O01_qi8zQuuceSvlLILcYt4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP917613.RARI4DwCAdMZ3nrMY6SKK8O01_qi8zQuuceSvlLILcYt4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP917613.RARI4DwCAdMZ3nrMY6SKK8O01_qi8zQuuceSvlLILcYt4130_provenance.
- NP917613.RARI4DwCAdMZ3nrMY6SKK8O01_qi8zQuuceSvlLILcYt4130_assertion description "[We describe a significant proportion of individual TS females having high levels of vWF, factor VIII, fibrinogen and CRP (15-40%) and an increased frequency of the Leiden mutation, with important associations with CIMT and blood pressure, suggesting that a subset of TS may have an unfavourable haemostatic balance, which may contribute to the increased risk of premature ischaemic heart disease and possibly increase the risk of deep venous and portal vein thrombosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917613.RARI4DwCAdMZ3nrMY6SKK8O01_qi8zQuuceSvlLILcYt4130_provenance.
- NP917613.RARI4DwCAdMZ3nrMY6SKK8O01_qi8zQuuceSvlLILcYt4130_assertion evidence source_evidence_literature NP917613.RARI4DwCAdMZ3nrMY6SKK8O01_qi8zQuuceSvlLILcYt4130_provenance.
- NP917613.RARI4DwCAdMZ3nrMY6SKK8O01_qi8zQuuceSvlLILcYt4130_assertion SIO_000772 21848660 NP917613.RARI4DwCAdMZ3nrMY6SKK8O01_qi8zQuuceSvlLILcYt4130_provenance.
- NP917613.RARI4DwCAdMZ3nrMY6SKK8O01_qi8zQuuceSvlLILcYt4130_assertion wasDerivedFrom befree-2016 NP917613.RARI4DwCAdMZ3nrMY6SKK8O01_qi8zQuuceSvlLILcYt4130_provenance.
- NP917613.RARI4DwCAdMZ3nrMY6SKK8O01_qi8zQuuceSvlLILcYt4130_assertion wasGeneratedBy ECO_0000203 NP917613.RARI4DwCAdMZ3nrMY6SKK8O01_qi8zQuuceSvlLILcYt4130_provenance.
- befree-2016 importedOn "2016-02-19" NP917613.RARI4DwCAdMZ3nrMY6SKK8O01_qi8zQuuceSvlLILcYt4130_provenance.