Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP556047.RAL6l184gmbxTeO_Z900xRcT2c3xFuSDnugbqyKRkZbFs130_assertion> ?p ?o ?g. }
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- NP556047.RAL6l184gmbxTeO_Z900xRcT2c3xFuSDnugbqyKRkZbFs130_assertion type Assertion NP556047.RAL6l184gmbxTeO_Z900xRcT2c3xFuSDnugbqyKRkZbFs130_head.
- NP556047.RAL6l184gmbxTeO_Z900xRcT2c3xFuSDnugbqyKRkZbFs130_assertion wasGeneratedBy ECO_0000203 NP556047.RAL6l184gmbxTeO_Z900xRcT2c3xFuSDnugbqyKRkZbFs130_provenance.
- NP556047.RAL6l184gmbxTeO_Z900xRcT2c3xFuSDnugbqyKRkZbFs130_assertion wasDerivedFrom befree-2016 NP556047.RAL6l184gmbxTeO_Z900xRcT2c3xFuSDnugbqyKRkZbFs130_provenance.
- NP556047.RAL6l184gmbxTeO_Z900xRcT2c3xFuSDnugbqyKRkZbFs130_assertion SIO_000772 16791607 NP556047.RAL6l184gmbxTeO_Z900xRcT2c3xFuSDnugbqyKRkZbFs130_provenance.
- NP556047.RAL6l184gmbxTeO_Z900xRcT2c3xFuSDnugbqyKRkZbFs130_assertion evidence source_evidence_literature NP556047.RAL6l184gmbxTeO_Z900xRcT2c3xFuSDnugbqyKRkZbFs130_provenance.
- NP556047.RAL6l184gmbxTeO_Z900xRcT2c3xFuSDnugbqyKRkZbFs130_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." NP556047.RAL6l184gmbxTeO_Z900xRcT2c3xFuSDnugbqyKRkZbFs130_provenance.