Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP477695.RAX2aCpgThnBWLHtrENR6p-W1ZAGGvu448l7aIhrPUjvE130_assertion> ?p ?o ?g. }
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- NP477695.RAX2aCpgThnBWLHtrENR6p-W1ZAGGvu448l7aIhrPUjvE130_assertion type Assertion NP477695.RAX2aCpgThnBWLHtrENR6p-W1ZAGGvu448l7aIhrPUjvE130_head.
- NP477695.RAX2aCpgThnBWLHtrENR6p-W1ZAGGvu448l7aIhrPUjvE130_assertion description "[We enrolled 49 unrelated Caucasian women with a history of two consecutive or three to six nonconsecutive early pregnancy losses and 48 unrelated parous healthy controls without a history of pregnancy loss and evaluated them for the following genetic variants: the factor V Leiden and prothrombin G20210A gene mutations, the methylenetetrahydrofolate reductase C677T and A1298C polymorphisms, and the PAI-1 4G/5G and FXIII Val34Leu polymorphisms.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477695.RAX2aCpgThnBWLHtrENR6p-W1ZAGGvu448l7aIhrPUjvE130_provenance.
- NP477695.RAX2aCpgThnBWLHtrENR6p-W1ZAGGvu448l7aIhrPUjvE130_assertion evidence source_evidence_literature NP477695.RAX2aCpgThnBWLHtrENR6p-W1ZAGGvu448l7aIhrPUjvE130_provenance.
- NP477695.RAX2aCpgThnBWLHtrENR6p-W1ZAGGvu448l7aIhrPUjvE130_assertion SIO_000772 12816904 NP477695.RAX2aCpgThnBWLHtrENR6p-W1ZAGGvu448l7aIhrPUjvE130_provenance.
- NP477695.RAX2aCpgThnBWLHtrENR6p-W1ZAGGvu448l7aIhrPUjvE130_assertion wasDerivedFrom befree-20140225 NP477695.RAX2aCpgThnBWLHtrENR6p-W1ZAGGvu448l7aIhrPUjvE130_provenance.
- NP477695.RAX2aCpgThnBWLHtrENR6p-W1ZAGGvu448l7aIhrPUjvE130_assertion wasGeneratedBy ECO_0000203 NP477695.RAX2aCpgThnBWLHtrENR6p-W1ZAGGvu448l7aIhrPUjvE130_provenance.