Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP927287.RAP4vzrAV8S6ON7KLi-UrlLKtB0U-0XX46tvNNCGIdBVc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP927287.RAP4vzrAV8S6ON7KLi-UrlLKtB0U-0XX46tvNNCGIdBVc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP927287.RAP4vzrAV8S6ON7KLi-UrlLKtB0U-0XX46tvNNCGIdBVc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP927287.RAP4vzrAV8S6ON7KLi-UrlLKtB0U-0XX46tvNNCGIdBVc130_provenance.
- NP927287.RAP4vzrAV8S6ON7KLi-UrlLKtB0U-0XX46tvNNCGIdBVc130_assertion description "[Homozygous individuals usually develop purpura fulminans as newborns; heterozygous protein C-deficient individuals are at increased risk for venous thrombosis and pulmonary embolism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927287.RAP4vzrAV8S6ON7KLi-UrlLKtB0U-0XX46tvNNCGIdBVc130_provenance.
- NP927287.RAP4vzrAV8S6ON7KLi-UrlLKtB0U-0XX46tvNNCGIdBVc130_assertion evidence source_evidence_literature NP927287.RAP4vzrAV8S6ON7KLi-UrlLKtB0U-0XX46tvNNCGIdBVc130_provenance.
- NP927287.RAP4vzrAV8S6ON7KLi-UrlLKtB0U-0XX46tvNNCGIdBVc130_assertion SIO_000772 2195715 NP927287.RAP4vzrAV8S6ON7KLi-UrlLKtB0U-0XX46tvNNCGIdBVc130_provenance.
- NP927287.RAP4vzrAV8S6ON7KLi-UrlLKtB0U-0XX46tvNNCGIdBVc130_assertion wasDerivedFrom befree-2016 NP927287.RAP4vzrAV8S6ON7KLi-UrlLKtB0U-0XX46tvNNCGIdBVc130_provenance.
- NP927287.RAP4vzrAV8S6ON7KLi-UrlLKtB0U-0XX46tvNNCGIdBVc130_assertion wasGeneratedBy ECO_0000203 NP927287.RAP4vzrAV8S6ON7KLi-UrlLKtB0U-0XX46tvNNCGIdBVc130_provenance.
- befree-2016 importedOn "2016-02-19" NP927287.RAP4vzrAV8S6ON7KLi-UrlLKtB0U-0XX46tvNNCGIdBVc130_provenance.