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- NP873414.RA-d1WMchB658ejXT0d-PHDS_ILJNVw_U5GgiUKd6htZc130_assertion type Assertion NP873414.RA-d1WMchB658ejXT0d-PHDS_ILJNVw_U5GgiUKd6htZc130_head.
- NP873414.RA-d1WMchB658ejXT0d-PHDS_ILJNVw_U5GgiUKd6htZc130_assertion wasGeneratedBy ECO_0000203 NP873414.RA-d1WMchB658ejXT0d-PHDS_ILJNVw_U5GgiUKd6htZc130_provenance.
- NP873414.RA-d1WMchB658ejXT0d-PHDS_ILJNVw_U5GgiUKd6htZc130_assertion wasDerivedFrom befree-20140225 NP873414.RA-d1WMchB658ejXT0d-PHDS_ILJNVw_U5GgiUKd6htZc130_provenance.
- NP873414.RA-d1WMchB658ejXT0d-PHDS_ILJNVw_U5GgiUKd6htZc130_assertion SIO_000772 16791607 NP873414.RA-d1WMchB658ejXT0d-PHDS_ILJNVw_U5GgiUKd6htZc130_provenance.
- NP873414.RA-d1WMchB658ejXT0d-PHDS_ILJNVw_U5GgiUKd6htZc130_assertion evidence source_evidence_literature NP873414.RA-d1WMchB658ejXT0d-PHDS_ILJNVw_U5GgiUKd6htZc130_provenance.
- NP873414.RA-d1WMchB658ejXT0d-PHDS_ILJNVw_U5GgiUKd6htZc130_assertion description "[Based on the hypothesis that an inherited predilection to hypercoagulability may predispose to HSP or may mark those who develop acute clinical manifestations, we evaluated the possible roles of methylenetetrahydrofolate reductase (MTHFR) gene C677T, factor V (FV) gene G1691A (Leiden), and prothrombin gene G20210A polymorphisms in patients with HSP.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP873414.RA-d1WMchB658ejXT0d-PHDS_ILJNVw_U5GgiUKd6htZc130_provenance.