Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP906577.RAHp3NNi9lHQsSCAfQGCU6OpXqiG350HS591uOBNq7hZI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP906577.RAHp3NNi9lHQsSCAfQGCU6OpXqiG350HS591uOBNq7hZI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP906577.RAHp3NNi9lHQsSCAfQGCU6OpXqiG350HS591uOBNq7hZI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP906577.RAHp3NNi9lHQsSCAfQGCU6OpXqiG350HS591uOBNq7hZI130_provenance.
- NP906577.RAHp3NNi9lHQsSCAfQGCU6OpXqiG350HS591uOBNq7hZI130_assertion description "[JAK2 exon 12 mutation screening is indicated only in the presence of JAK2V617F-negative erythrocytosis that is associated with a subnormal serum erythropoietin level.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP906577.RAHp3NNi9lHQsSCAfQGCU6OpXqiG350HS591uOBNq7hZI130_provenance.
- NP906577.RAHp3NNi9lHQsSCAfQGCU6OpXqiG350HS591uOBNq7hZI130_assertion evidence source_evidence_literature NP906577.RAHp3NNi9lHQsSCAfQGCU6OpXqiG350HS591uOBNq7hZI130_provenance.
- NP906577.RAHp3NNi9lHQsSCAfQGCU6OpXqiG350HS591uOBNq7hZI130_assertion SIO_000772 21723416 NP906577.RAHp3NNi9lHQsSCAfQGCU6OpXqiG350HS591uOBNq7hZI130_provenance.
- NP906577.RAHp3NNi9lHQsSCAfQGCU6OpXqiG350HS591uOBNq7hZI130_assertion wasDerivedFrom befree-2016 NP906577.RAHp3NNi9lHQsSCAfQGCU6OpXqiG350HS591uOBNq7hZI130_provenance.
- NP906577.RAHp3NNi9lHQsSCAfQGCU6OpXqiG350HS591uOBNq7hZI130_assertion wasGeneratedBy ECO_0000203 NP906577.RAHp3NNi9lHQsSCAfQGCU6OpXqiG350HS591uOBNq7hZI130_provenance.
- befree-2016 importedOn "2016-02-19" NP906577.RAHp3NNi9lHQsSCAfQGCU6OpXqiG350HS591uOBNq7hZI130_provenance.