Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP675496.RAc57ycgOnWI3isW0rETsmwCmWseAFlpJcs6Dgvw9ZnMk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP675496.RAc57ycgOnWI3isW0rETsmwCmWseAFlpJcs6Dgvw9ZnMk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP675496.RAc57ycgOnWI3isW0rETsmwCmWseAFlpJcs6Dgvw9ZnMk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP675496.RAc57ycgOnWI3isW0rETsmwCmWseAFlpJcs6Dgvw9ZnMk130_provenance.
- befree-2016 importedOn "2016-02-19" NP675496.RAc57ycgOnWI3isW0rETsmwCmWseAFlpJcs6Dgvw9ZnMk130_provenance.
- NP675496.RAc57ycgOnWI3isW0rETsmwCmWseAFlpJcs6Dgvw9ZnMk130_assertion wasGeneratedBy ECO_0000203 NP675496.RAc57ycgOnWI3isW0rETsmwCmWseAFlpJcs6Dgvw9ZnMk130_provenance.
- NP675496.RAc57ycgOnWI3isW0rETsmwCmWseAFlpJcs6Dgvw9ZnMk130_assertion wasDerivedFrom befree-2016 NP675496.RAc57ycgOnWI3isW0rETsmwCmWseAFlpJcs6Dgvw9ZnMk130_provenance.
- NP675496.RAc57ycgOnWI3isW0rETsmwCmWseAFlpJcs6Dgvw9ZnMk130_assertion SIO_000772 18538168 NP675496.RAc57ycgOnWI3isW0rETsmwCmWseAFlpJcs6Dgvw9ZnMk130_provenance.
- NP675496.RAc57ycgOnWI3isW0rETsmwCmWseAFlpJcs6Dgvw9ZnMk130_assertion evidence source_evidence_literature NP675496.RAc57ycgOnWI3isW0rETsmwCmWseAFlpJcs6Dgvw9ZnMk130_provenance.
- NP675496.RAc57ycgOnWI3isW0rETsmwCmWseAFlpJcs6Dgvw9ZnMk130_assertion description "[This review aims to summarize the discovery and use of the JAK2V617F point mutation, other novel JAK2 mutations, and JAK2 translocations in diagnosing myeloproliferative neoplasms, acute myeloid leukemia, and acute lymphoid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP675496.RAc57ycgOnWI3isW0rETsmwCmWseAFlpJcs6Dgvw9ZnMk130_provenance.