Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP894359.RAQ0mKtbpJGq82LBR2cz9ZLQGktD0p77tnC-GAjniWDho130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP894359.RAQ0mKtbpJGq82LBR2cz9ZLQGktD0p77tnC-GAjniWDho130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP894359.RAQ0mKtbpJGq82LBR2cz9ZLQGktD0p77tnC-GAjniWDho130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP894359.RAQ0mKtbpJGq82LBR2cz9ZLQGktD0p77tnC-GAjniWDho130_provenance.
- NP894359.RAQ0mKtbpJGq82LBR2cz9ZLQGktD0p77tnC-GAjniWDho130_assertion description "[In the present study, we screened for protein C amidolytic activity in patients admitted to the National Cardiovascular Center Hospital, and we identified among them 43 probands and 51 relatives with heterozygous protein C deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP894359.RAQ0mKtbpJGq82LBR2cz9ZLQGktD0p77tnC-GAjniWDho130_provenance.
- NP894359.RAQ0mKtbpJGq82LBR2cz9ZLQGktD0p77tnC-GAjniWDho130_assertion evidence source_evidence_literature NP894359.RAQ0mKtbpJGq82LBR2cz9ZLQGktD0p77tnC-GAjniWDho130_provenance.
- NP894359.RAQ0mKtbpJGq82LBR2cz9ZLQGktD0p77tnC-GAjniWDho130_assertion SIO_000772 10230891 NP894359.RAQ0mKtbpJGq82LBR2cz9ZLQGktD0p77tnC-GAjniWDho130_provenance.
- NP894359.RAQ0mKtbpJGq82LBR2cz9ZLQGktD0p77tnC-GAjniWDho130_assertion wasDerivedFrom befree-20140225 NP894359.RAQ0mKtbpJGq82LBR2cz9ZLQGktD0p77tnC-GAjniWDho130_provenance.
- NP894359.RAQ0mKtbpJGq82LBR2cz9ZLQGktD0p77tnC-GAjniWDho130_assertion wasGeneratedBy ECO_0000203 NP894359.RAQ0mKtbpJGq82LBR2cz9ZLQGktD0p77tnC-GAjniWDho130_provenance.
- befree-20140225 importedOn "2014-02-25" NP894359.RAQ0mKtbpJGq82LBR2cz9ZLQGktD0p77tnC-GAjniWDho130_provenance.