Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP100019.RAlgYzcde04Asy0oMGgmO2iTnTXH3o18fLLW11M-OTaqU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP100019.RAlgYzcde04Asy0oMGgmO2iTnTXH3o18fLLW11M-OTaqU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP100019.RAlgYzcde04Asy0oMGgmO2iTnTXH3o18fLLW11M-OTaqU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP100019.RAlgYzcde04Asy0oMGgmO2iTnTXH3o18fLLW11M-OTaqU130_provenance.
- NP100019.RAlgYzcde04Asy0oMGgmO2iTnTXH3o18fLLW11M-OTaqU130_assertion description "[FVL mutation is a significant risk factor for pregnancy complications and adverse outcomes, and MTHFR 677CT/TT genotype can further enhance the risk of stillbirth.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP100019.RAlgYzcde04Asy0oMGgmO2iTnTXH3o18fLLW11M-OTaqU130_provenance.
- NP100019.RAlgYzcde04Asy0oMGgmO2iTnTXH3o18fLLW11M-OTaqU130_assertion evidence source_evidence_literature NP100019.RAlgYzcde04Asy0oMGgmO2iTnTXH3o18fLLW11M-OTaqU130_provenance.
- NP100019.RAlgYzcde04Asy0oMGgmO2iTnTXH3o18fLLW11M-OTaqU130_assertion SIO_000772 16613994 NP100019.RAlgYzcde04Asy0oMGgmO2iTnTXH3o18fLLW11M-OTaqU130_provenance.
- NP100019.RAlgYzcde04Asy0oMGgmO2iTnTXH3o18fLLW11M-OTaqU130_assertion wasDerivedFrom gad-20150221 NP100019.RAlgYzcde04Asy0oMGgmO2iTnTXH3o18fLLW11M-OTaqU130_provenance.
- NP100019.RAlgYzcde04Asy0oMGgmO2iTnTXH3o18fLLW11M-OTaqU130_assertion wasGeneratedBy ECO_0000203 NP100019.RAlgYzcde04Asy0oMGgmO2iTnTXH3o18fLLW11M-OTaqU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP100019.RAlgYzcde04Asy0oMGgmO2iTnTXH3o18fLLW11M-OTaqU130_provenance.