Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1259776.RAHazsVNimjEbo4L56sznxC8757mxhb3bU534UCLGnevM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1259776.RAHazsVNimjEbo4L56sznxC8757mxhb3bU534UCLGnevM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1259776.RAHazsVNimjEbo4L56sznxC8757mxhb3bU534UCLGnevM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1259776.RAHazsVNimjEbo4L56sznxC8757mxhb3bU534UCLGnevM130_provenance.
- NP1259776.RAHazsVNimjEbo4L56sznxC8757mxhb3bU534UCLGnevM130_assertion description "[Despite its small size, the study shows much less prevalence of JAK2 mutation in PV, ET and MF, which does not match international data.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1259776.RAHazsVNimjEbo4L56sznxC8757mxhb3bU534UCLGnevM130_provenance.
- NP1259776.RAHazsVNimjEbo4L56sznxC8757mxhb3bU534UCLGnevM130_assertion evidence source_evidence_literature NP1259776.RAHazsVNimjEbo4L56sznxC8757mxhb3bU534UCLGnevM130_provenance.
- NP1259776.RAHazsVNimjEbo4L56sznxC8757mxhb3bU534UCLGnevM130_assertion SIO_000772 25637689 NP1259776.RAHazsVNimjEbo4L56sznxC8757mxhb3bU534UCLGnevM130_provenance.
- NP1259776.RAHazsVNimjEbo4L56sznxC8757mxhb3bU534UCLGnevM130_assertion wasDerivedFrom befree-2016 NP1259776.RAHazsVNimjEbo4L56sznxC8757mxhb3bU534UCLGnevM130_provenance.
- NP1259776.RAHazsVNimjEbo4L56sznxC8757mxhb3bU534UCLGnevM130_assertion wasGeneratedBy ECO_0000203 NP1259776.RAHazsVNimjEbo4L56sznxC8757mxhb3bU534UCLGnevM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1259776.RAHazsVNimjEbo4L56sznxC8757mxhb3bU534UCLGnevM130_provenance.