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- source_evidence_literature type ECO_0000212 NP398826.RAVoY2dmh-A364TI06WRPgWxLdAJKMAeL3aqCT_uzK5zI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP398826.RAVoY2dmh-A364TI06WRPgWxLdAJKMAeL3aqCT_uzK5zI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP398826.RAVoY2dmh-A364TI06WRPgWxLdAJKMAeL3aqCT_uzK5zI130_provenance.
- NP398826.RAVoY2dmh-A364TI06WRPgWxLdAJKMAeL3aqCT_uzK5zI130_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." NP398826.RAVoY2dmh-A364TI06WRPgWxLdAJKMAeL3aqCT_uzK5zI130_provenance.
- NP398826.RAVoY2dmh-A364TI06WRPgWxLdAJKMAeL3aqCT_uzK5zI130_assertion evidence source_evidence_literature NP398826.RAVoY2dmh-A364TI06WRPgWxLdAJKMAeL3aqCT_uzK5zI130_provenance.
- NP398826.RAVoY2dmh-A364TI06WRPgWxLdAJKMAeL3aqCT_uzK5zI130_assertion SIO_000772 12816904 NP398826.RAVoY2dmh-A364TI06WRPgWxLdAJKMAeL3aqCT_uzK5zI130_provenance.
- NP398826.RAVoY2dmh-A364TI06WRPgWxLdAJKMAeL3aqCT_uzK5zI130_assertion wasDerivedFrom befree-2016 NP398826.RAVoY2dmh-A364TI06WRPgWxLdAJKMAeL3aqCT_uzK5zI130_provenance.
- NP398826.RAVoY2dmh-A364TI06WRPgWxLdAJKMAeL3aqCT_uzK5zI130_assertion wasGeneratedBy ECO_0000203 NP398826.RAVoY2dmh-A364TI06WRPgWxLdAJKMAeL3aqCT_uzK5zI130_provenance.
- befree-2016 importedOn "2016-02-19" NP398826.RAVoY2dmh-A364TI06WRPgWxLdAJKMAeL3aqCT_uzK5zI130_provenance.