Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP427841.RAZbNdibdIpJQ5CVQs24LzDh9P7N1Axhg92HS6ibpq2Hw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP427841.RAZbNdibdIpJQ5CVQs24LzDh9P7N1Axhg92HS6ibpq2Hw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP427841.RAZbNdibdIpJQ5CVQs24LzDh9P7N1Axhg92HS6ibpq2Hw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP427841.RAZbNdibdIpJQ5CVQs24LzDh9P7N1Axhg92HS6ibpq2Hw130_provenance.
- NP427841.RAZbNdibdIpJQ5CVQs24LzDh9P7N1Axhg92HS6ibpq2Hw130_assertion description "[However, in primiparous patients, the frequency was significantly different in elderly pregnancy (63% in severe HP vs. 18% in controls; P < 0.05), in the subgroup with the MM+MT genotypes of the angiotensinogen gene (50% in severe HP vs. 26% in controls; P < 0.05), and in the subgroup with the GA+AA genotypes of the endothelial nitric oxide synthase gene (42% in severe HP vs. 13% in controls; P < 0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427841.RAZbNdibdIpJQ5CVQs24LzDh9P7N1Axhg92HS6ibpq2Hw130_provenance.
- NP427841.RAZbNdibdIpJQ5CVQs24LzDh9P7N1Axhg92HS6ibpq2Hw130_assertion evidence source_evidence_literature NP427841.RAZbNdibdIpJQ5CVQs24LzDh9P7N1Axhg92HS6ibpq2Hw130_provenance.
- NP427841.RAZbNdibdIpJQ5CVQs24LzDh9P7N1Axhg92HS6ibpq2Hw130_assertion SIO_000772 14719182 NP427841.RAZbNdibdIpJQ5CVQs24LzDh9P7N1Axhg92HS6ibpq2Hw130_provenance.
- NP427841.RAZbNdibdIpJQ5CVQs24LzDh9P7N1Axhg92HS6ibpq2Hw130_assertion wasDerivedFrom befree-2016 NP427841.RAZbNdibdIpJQ5CVQs24LzDh9P7N1Axhg92HS6ibpq2Hw130_provenance.
- NP427841.RAZbNdibdIpJQ5CVQs24LzDh9P7N1Axhg92HS6ibpq2Hw130_assertion wasGeneratedBy ECO_0000203 NP427841.RAZbNdibdIpJQ5CVQs24LzDh9P7N1Axhg92HS6ibpq2Hw130_provenance.
- befree-2016 importedOn "2016-02-19" NP427841.RAZbNdibdIpJQ5CVQs24LzDh9P7N1Axhg92HS6ibpq2Hw130_provenance.