Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP391786.RAOKTSpZcXZvDU1GdUAV5FxAqbI2k7mxS2RKGhALXDd2M130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP391786.RAOKTSpZcXZvDU1GdUAV5FxAqbI2k7mxS2RKGhALXDd2M130_assertion type Assertion NP391786.RAOKTSpZcXZvDU1GdUAV5FxAqbI2k7mxS2RKGhALXDd2M130_head.
- NP391786.RAOKTSpZcXZvDU1GdUAV5FxAqbI2k7mxS2RKGhALXDd2M130_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." NP391786.RAOKTSpZcXZvDU1GdUAV5FxAqbI2k7mxS2RKGhALXDd2M130_provenance.
- NP391786.RAOKTSpZcXZvDU1GdUAV5FxAqbI2k7mxS2RKGhALXDd2M130_assertion evidence source_evidence_literature NP391786.RAOKTSpZcXZvDU1GdUAV5FxAqbI2k7mxS2RKGhALXDd2M130_provenance.
- NP391786.RAOKTSpZcXZvDU1GdUAV5FxAqbI2k7mxS2RKGhALXDd2M130_assertion SIO_000772 12816904 NP391786.RAOKTSpZcXZvDU1GdUAV5FxAqbI2k7mxS2RKGhALXDd2M130_provenance.
- NP391786.RAOKTSpZcXZvDU1GdUAV5FxAqbI2k7mxS2RKGhALXDd2M130_assertion wasDerivedFrom befree-20150227 NP391786.RAOKTSpZcXZvDU1GdUAV5FxAqbI2k7mxS2RKGhALXDd2M130_provenance.
- NP391786.RAOKTSpZcXZvDU1GdUAV5FxAqbI2k7mxS2RKGhALXDd2M130_assertion wasGeneratedBy ECO_0000203 NP391786.RAOKTSpZcXZvDU1GdUAV5FxAqbI2k7mxS2RKGhALXDd2M130_provenance.