Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP691368.RADvx_01fpcSxSE9WRdVZlTcRRY096v1K0LVC4WGCfVtc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP691368.RADvx_01fpcSxSE9WRdVZlTcRRY096v1K0LVC4WGCfVtc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP691368.RADvx_01fpcSxSE9WRdVZlTcRRY096v1K0LVC4WGCfVtc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP691368.RADvx_01fpcSxSE9WRdVZlTcRRY096v1K0LVC4WGCfVtc130_provenance.
- NP691368.RADvx_01fpcSxSE9WRdVZlTcRRY096v1K0LVC4WGCfVtc130_assertion description "[We used the thrombin generation assay to evaluate the hypercoagulable state according to JAK2(V617F) mutational status in essential thrombocythemia (ET) and polycythemia vera (PV) patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691368.RADvx_01fpcSxSE9WRdVZlTcRRY096v1K0LVC4WGCfVtc130_provenance.
- NP691368.RADvx_01fpcSxSE9WRdVZlTcRRY096v1K0LVC4WGCfVtc130_assertion evidence source_evidence_literature NP691368.RADvx_01fpcSxSE9WRdVZlTcRRY096v1K0LVC4WGCfVtc130_provenance.
- NP691368.RADvx_01fpcSxSE9WRdVZlTcRRY096v1K0LVC4WGCfVtc130_assertion SIO_000772 18768782 NP691368.RADvx_01fpcSxSE9WRdVZlTcRRY096v1K0LVC4WGCfVtc130_provenance.
- NP691368.RADvx_01fpcSxSE9WRdVZlTcRRY096v1K0LVC4WGCfVtc130_assertion wasDerivedFrom befree-2016 NP691368.RADvx_01fpcSxSE9WRdVZlTcRRY096v1K0LVC4WGCfVtc130_provenance.
- NP691368.RADvx_01fpcSxSE9WRdVZlTcRRY096v1K0LVC4WGCfVtc130_assertion wasGeneratedBy ECO_0000203 NP691368.RADvx_01fpcSxSE9WRdVZlTcRRY096v1K0LVC4WGCfVtc130_provenance.
- befree-2016 importedOn "2016-02-19" NP691368.RADvx_01fpcSxSE9WRdVZlTcRRY096v1K0LVC4WGCfVtc130_provenance.