Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1198145.RAs8qCkCv2frepPy72066KTJmNBdHq90d0ErJwiNdvYkw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1198145.RAs8qCkCv2frepPy72066KTJmNBdHq90d0ErJwiNdvYkw130_assertion type Assertion NP1198145.RAs8qCkCv2frepPy72066KTJmNBdHq90d0ErJwiNdvYkw130_head.
- NP1198145.RAs8qCkCv2frepPy72066KTJmNBdHq90d0ErJwiNdvYkw130_assertion wasGeneratedBy ECO_0000203 NP1198145.RAs8qCkCv2frepPy72066KTJmNBdHq90d0ErJwiNdvYkw130_provenance.
- NP1198145.RAs8qCkCv2frepPy72066KTJmNBdHq90d0ErJwiNdvYkw130_assertion wasDerivedFrom befree-2016 NP1198145.RAs8qCkCv2frepPy72066KTJmNBdHq90d0ErJwiNdvYkw130_provenance.
- NP1198145.RAs8qCkCv2frepPy72066KTJmNBdHq90d0ErJwiNdvYkw130_assertion SIO_000772 24991435 NP1198145.RAs8qCkCv2frepPy72066KTJmNBdHq90d0ErJwiNdvYkw130_provenance.
- NP1198145.RAs8qCkCv2frepPy72066KTJmNBdHq90d0ErJwiNdvYkw130_assertion evidence source_evidence_literature NP1198145.RAs8qCkCv2frepPy72066KTJmNBdHq90d0ErJwiNdvYkw130_provenance.
- NP1198145.RAs8qCkCv2frepPy72066KTJmNBdHq90d0ErJwiNdvYkw130_assertion description "[Carriers of the TT and the CC genotype of the MTHFR C677T polymorphism seem to have an increased risk of the HELLP syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1198145.RAs8qCkCv2frepPy72066KTJmNBdHq90d0ErJwiNdvYkw130_provenance.