Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP389791.RAl-dorYEe62R8HYJFgv5jEPMYr4K0dIC7PGPakQ5KD-U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP389791.RAl-dorYEe62R8HYJFgv5jEPMYr4K0dIC7PGPakQ5KD-U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP389791.RAl-dorYEe62R8HYJFgv5jEPMYr4K0dIC7PGPakQ5KD-U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP389791.RAl-dorYEe62R8HYJFgv5jEPMYr4K0dIC7PGPakQ5KD-U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP389791.RAl-dorYEe62R8HYJFgv5jEPMYr4K0dIC7PGPakQ5KD-U130_provenance.
- NP389791.RAl-dorYEe62R8HYJFgv5jEPMYr4K0dIC7PGPakQ5KD-U130_assertion wasGeneratedBy ECO_0000203 NP389791.RAl-dorYEe62R8HYJFgv5jEPMYr4K0dIC7PGPakQ5KD-U130_provenance.
- NP389791.RAl-dorYEe62R8HYJFgv5jEPMYr4K0dIC7PGPakQ5KD-U130_assertion wasDerivedFrom befree-20150227 NP389791.RAl-dorYEe62R8HYJFgv5jEPMYr4K0dIC7PGPakQ5KD-U130_provenance.
- NP389791.RAl-dorYEe62R8HYJFgv5jEPMYr4K0dIC7PGPakQ5KD-U130_assertion SIO_000772 16392896 NP389791.RAl-dorYEe62R8HYJFgv5jEPMYr4K0dIC7PGPakQ5KD-U130_provenance.
- NP389791.RAl-dorYEe62R8HYJFgv5jEPMYr4K0dIC7PGPakQ5KD-U130_assertion evidence source_evidence_literature NP389791.RAl-dorYEe62R8HYJFgv5jEPMYr4K0dIC7PGPakQ5KD-U130_provenance.
- NP389791.RAl-dorYEe62R8HYJFgv5jEPMYr4K0dIC7PGPakQ5KD-U130_assertion description "[Testing should be based on the phenotype for antithrombin, protein C and protein S; on the phenotype and genotype (factor V Leiden mutation) for activated protein C resistance; and on the genotype (G20210A mutation) for hyperprothrombinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP389791.RAl-dorYEe62R8HYJFgv5jEPMYr4K0dIC7PGPakQ5KD-U130_provenance.