Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1405229.RAd7RKw5MvdNj1phIMBfviUcff6L3GF6BTJc9sVT_ES6g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1405229.RAd7RKw5MvdNj1phIMBfviUcff6L3GF6BTJc9sVT_ES6g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1405229.RAd7RKw5MvdNj1phIMBfviUcff6L3GF6BTJc9sVT_ES6g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1405229.RAd7RKw5MvdNj1phIMBfviUcff6L3GF6BTJc9sVT_ES6g130_provenance.
- NP1405229.RAd7RKw5MvdNj1phIMBfviUcff6L3GF6BTJc9sVT_ES6g130_assertion description "[Laboratory assays are currently available to diagnose and type hereditary thrombophilia due to deficiency or dysfunction of one of the anticoagulant factors antithrombin (AT), protein C (PC) and protein S (PS), and APC resistance without the need of DNA analysis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1405229.RAd7RKw5MvdNj1phIMBfviUcff6L3GF6BTJc9sVT_ES6g130_provenance.
- NP1405229.RAd7RKw5MvdNj1phIMBfviUcff6L3GF6BTJc9sVT_ES6g130_assertion evidence source_evidence_literature NP1405229.RAd7RKw5MvdNj1phIMBfviUcff6L3GF6BTJc9sVT_ES6g130_provenance.
- NP1405229.RAd7RKw5MvdNj1phIMBfviUcff6L3GF6BTJc9sVT_ES6g130_assertion SIO_000772 9763348 NP1405229.RAd7RKw5MvdNj1phIMBfviUcff6L3GF6BTJc9sVT_ES6g130_provenance.
- NP1405229.RAd7RKw5MvdNj1phIMBfviUcff6L3GF6BTJc9sVT_ES6g130_assertion wasDerivedFrom befree-2016 NP1405229.RAd7RKw5MvdNj1phIMBfviUcff6L3GF6BTJc9sVT_ES6g130_provenance.
- NP1405229.RAd7RKw5MvdNj1phIMBfviUcff6L3GF6BTJc9sVT_ES6g130_assertion wasGeneratedBy ECO_0000203 NP1405229.RAd7RKw5MvdNj1phIMBfviUcff6L3GF6BTJc9sVT_ES6g130_provenance.
- befree-2016 importedOn "2016-02-19" NP1405229.RAd7RKw5MvdNj1phIMBfviUcff6L3GF6BTJc9sVT_ES6g130_provenance.