Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP734144.RAFK-_4O5TmpAcMhAW4OPkZzuZvamBh1AJtiZKV9pnpc8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP734144.RAFK-_4O5TmpAcMhAW4OPkZzuZvamBh1AJtiZKV9pnpc8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734144.RAFK-_4O5TmpAcMhAW4OPkZzuZvamBh1AJtiZKV9pnpc8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734144.RAFK-_4O5TmpAcMhAW4OPkZzuZvamBh1AJtiZKV9pnpc8130_provenance.
- NP734144.RAFK-_4O5TmpAcMhAW4OPkZzuZvamBh1AJtiZKV9pnpc8130_assertion description "[To the best of our knowledge this is the first report of CDKN1C mutations in children born to women with preeclampsia/HELLP syndrome, thus suggesting the involvement of an imprinted gene in the pathophysiology of preeclampsia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP734144.RAFK-_4O5TmpAcMhAW4OPkZzuZvamBh1AJtiZKV9pnpc8130_provenance.
- NP734144.RAFK-_4O5TmpAcMhAW4OPkZzuZvamBh1AJtiZKV9pnpc8130_assertion evidence source_evidence_literature NP734144.RAFK-_4O5TmpAcMhAW4OPkZzuZvamBh1AJtiZKV9pnpc8130_provenance.
- NP734144.RAFK-_4O5TmpAcMhAW4OPkZzuZvamBh1AJtiZKV9pnpc8130_assertion SIO_000772 19386358 NP734144.RAFK-_4O5TmpAcMhAW4OPkZzuZvamBh1AJtiZKV9pnpc8130_provenance.
- NP734144.RAFK-_4O5TmpAcMhAW4OPkZzuZvamBh1AJtiZKV9pnpc8130_assertion wasDerivedFrom befree-2016 NP734144.RAFK-_4O5TmpAcMhAW4OPkZzuZvamBh1AJtiZKV9pnpc8130_provenance.
- NP734144.RAFK-_4O5TmpAcMhAW4OPkZzuZvamBh1AJtiZKV9pnpc8130_assertion wasGeneratedBy ECO_0000203 NP734144.RAFK-_4O5TmpAcMhAW4OPkZzuZvamBh1AJtiZKV9pnpc8130_provenance.
- befree-2016 importedOn "2016-02-19" NP734144.RAFK-_4O5TmpAcMhAW4OPkZzuZvamBh1AJtiZKV9pnpc8130_provenance.