Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP226867.RAuSaVd9_zce32XjPqL3ibwCpJJHqiDIYZVzZ82GFuduQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP226867.RAuSaVd9_zce32XjPqL3ibwCpJJHqiDIYZVzZ82GFuduQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP226867.RAuSaVd9_zce32XjPqL3ibwCpJJHqiDIYZVzZ82GFuduQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP226867.RAuSaVd9_zce32XjPqL3ibwCpJJHqiDIYZVzZ82GFuduQ130_provenance.
- NP226867.RAuSaVd9_zce32XjPqL3ibwCpJJHqiDIYZVzZ82GFuduQ130_assertion description "[TET2 deletions are a recurrent but rare phenomenon in myeloid malignancies and are frequently accompanied by TET2 mutations on the remaining allele.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP226867.RAuSaVd9_zce32XjPqL3ibwCpJJHqiDIYZVzZ82GFuduQ130_provenance.
- NP226867.RAuSaVd9_zce32XjPqL3ibwCpJJHqiDIYZVzZ82GFuduQ130_assertion evidence source_evidence_literature NP226867.RAuSaVd9_zce32XjPqL3ibwCpJJHqiDIYZVzZ82GFuduQ130_provenance.
- NP226867.RAuSaVd9_zce32XjPqL3ibwCpJJHqiDIYZVzZ82GFuduQ130_assertion SIO_000772 22017486 NP226867.RAuSaVd9_zce32XjPqL3ibwCpJJHqiDIYZVzZ82GFuduQ130_provenance.
- NP226867.RAuSaVd9_zce32XjPqL3ibwCpJJHqiDIYZVzZ82GFuduQ130_assertion wasDerivedFrom befree-20140225 NP226867.RAuSaVd9_zce32XjPqL3ibwCpJJHqiDIYZVzZ82GFuduQ130_provenance.
- NP226867.RAuSaVd9_zce32XjPqL3ibwCpJJHqiDIYZVzZ82GFuduQ130_assertion wasGeneratedBy ECO_0000203 NP226867.RAuSaVd9_zce32XjPqL3ibwCpJJHqiDIYZVzZ82GFuduQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP226867.RAuSaVd9_zce32XjPqL3ibwCpJJHqiDIYZVzZ82GFuduQ130_provenance.