Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP582323.RA7fS5_vl2haUpNiCCxpZ6oERjPNfo63Da1jXwd0WhnRo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP582323.RA7fS5_vl2haUpNiCCxpZ6oERjPNfo63Da1jXwd0WhnRo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP582323.RA7fS5_vl2haUpNiCCxpZ6oERjPNfo63Da1jXwd0WhnRo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP582323.RA7fS5_vl2haUpNiCCxpZ6oERjPNfo63Da1jXwd0WhnRo130_provenance.
- NP582323.RA7fS5_vl2haUpNiCCxpZ6oERjPNfo63Da1jXwd0WhnRo130_assertion description "[JAK2V617F mutation screening is indicated for the evaluation of erythrocytosis, thrombocytosis, splanchnic vein thrombosis, and otherwise unexplained BCR-ABL1-negative granulocytosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP582323.RA7fS5_vl2haUpNiCCxpZ6oERjPNfo63Da1jXwd0WhnRo130_provenance.
- NP582323.RA7fS5_vl2haUpNiCCxpZ6oERjPNfo63Da1jXwd0WhnRo130_assertion evidence source_evidence_literature NP582323.RA7fS5_vl2haUpNiCCxpZ6oERjPNfo63Da1jXwd0WhnRo130_provenance.
- NP582323.RA7fS5_vl2haUpNiCCxpZ6oERjPNfo63Da1jXwd0WhnRo130_assertion SIO_000772 21723416 NP582323.RA7fS5_vl2haUpNiCCxpZ6oERjPNfo63Da1jXwd0WhnRo130_provenance.
- NP582323.RA7fS5_vl2haUpNiCCxpZ6oERjPNfo63Da1jXwd0WhnRo130_assertion wasDerivedFrom befree-20140225 NP582323.RA7fS5_vl2haUpNiCCxpZ6oERjPNfo63Da1jXwd0WhnRo130_provenance.
- NP582323.RA7fS5_vl2haUpNiCCxpZ6oERjPNfo63Da1jXwd0WhnRo130_assertion wasGeneratedBy ECO_0000203 NP582323.RA7fS5_vl2haUpNiCCxpZ6oERjPNfo63Da1jXwd0WhnRo130_provenance.
- befree-20140225 importedOn "2014-02-25" NP582323.RA7fS5_vl2haUpNiCCxpZ6oERjPNfo63Da1jXwd0WhnRo130_provenance.