Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1302806.RAdLPkkaduiIT2kwJFhFwhdIEA-2T5HX5JLID8l03v0gk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1302806.RAdLPkkaduiIT2kwJFhFwhdIEA-2T5HX5JLID8l03v0gk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1302806.RAdLPkkaduiIT2kwJFhFwhdIEA-2T5HX5JLID8l03v0gk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1302806.RAdLPkkaduiIT2kwJFhFwhdIEA-2T5HX5JLID8l03v0gk130_provenance.
- NP1302806.RAdLPkkaduiIT2kwJFhFwhdIEA-2T5HX5JLID8l03v0gk130_assertion description "[In newborns with homozygous protein C deficiency with very low protein C levels (1%) a purpura fulminans like syndrome was observed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1302806.RAdLPkkaduiIT2kwJFhFwhdIEA-2T5HX5JLID8l03v0gk130_provenance.
- NP1302806.RAdLPkkaduiIT2kwJFhFwhdIEA-2T5HX5JLID8l03v0gk130_assertion evidence source_evidence_literature NP1302806.RAdLPkkaduiIT2kwJFhFwhdIEA-2T5HX5JLID8l03v0gk130_provenance.
- NP1302806.RAdLPkkaduiIT2kwJFhFwhdIEA-2T5HX5JLID8l03v0gk130_assertion SIO_000772 3524711 NP1302806.RAdLPkkaduiIT2kwJFhFwhdIEA-2T5HX5JLID8l03v0gk130_provenance.
- NP1302806.RAdLPkkaduiIT2kwJFhFwhdIEA-2T5HX5JLID8l03v0gk130_assertion wasDerivedFrom befree-2016 NP1302806.RAdLPkkaduiIT2kwJFhFwhdIEA-2T5HX5JLID8l03v0gk130_provenance.
- NP1302806.RAdLPkkaduiIT2kwJFhFwhdIEA-2T5HX5JLID8l03v0gk130_assertion wasGeneratedBy ECO_0000203 NP1302806.RAdLPkkaduiIT2kwJFhFwhdIEA-2T5HX5JLID8l03v0gk130_provenance.
- befree-2016 importedOn "2016-02-19" NP1302806.RAdLPkkaduiIT2kwJFhFwhdIEA-2T5HX5JLID8l03v0gk130_provenance.