Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_provenance.
- befree-2016 importedOn "2016-02-19" NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_provenance.
- NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_assertion wasGeneratedBy ECO_0000203 NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_provenance.
- NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_assertion wasDerivedFrom befree-2016 NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_provenance.
- NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_assertion SIO_000772 16931578 NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_provenance.
- NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_assertion evidence source_evidence_literature NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_provenance.
- NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_assertion description "[The V617F mutation is present in blood and marrow from a large proportion of patients with classic BCR/ABL-negative chronic myeloproliferative disorders and of a few patients with other clonal hematological diseases such as myelodysplastic syndrome, atypical myeloproliferative disorders, and acute myeloid leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP565908.RAouO6HNLgirFKwX_NBEBG5DvaQD3tHqf6yvPknEyt0hM130_provenance.