Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP219247.RAfNXP2SmjmGq1b8EXi-y0rYU07xGPmvxZ0o9kZDHe5uQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP219247.RAfNXP2SmjmGq1b8EXi-y0rYU07xGPmvxZ0o9kZDHe5uQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP219247.RAfNXP2SmjmGq1b8EXi-y0rYU07xGPmvxZ0o9kZDHe5uQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP219247.RAfNXP2SmjmGq1b8EXi-y0rYU07xGPmvxZ0o9kZDHe5uQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP219247.RAfNXP2SmjmGq1b8EXi-y0rYU07xGPmvxZ0o9kZDHe5uQ130_provenance.
- NP219247.RAfNXP2SmjmGq1b8EXi-y0rYU07xGPmvxZ0o9kZDHe5uQ130_assertion wasGeneratedBy ECO_0000203 NP219247.RAfNXP2SmjmGq1b8EXi-y0rYU07xGPmvxZ0o9kZDHe5uQ130_provenance.
- NP219247.RAfNXP2SmjmGq1b8EXi-y0rYU07xGPmvxZ0o9kZDHe5uQ130_assertion wasDerivedFrom befree-20150227 NP219247.RAfNXP2SmjmGq1b8EXi-y0rYU07xGPmvxZ0o9kZDHe5uQ130_provenance.
- NP219247.RAfNXP2SmjmGq1b8EXi-y0rYU07xGPmvxZ0o9kZDHe5uQ130_assertion SIO_000772 16931578 NP219247.RAfNXP2SmjmGq1b8EXi-y0rYU07xGPmvxZ0o9kZDHe5uQ130_provenance.
- NP219247.RAfNXP2SmjmGq1b8EXi-y0rYU07xGPmvxZ0o9kZDHe5uQ130_assertion evidence source_evidence_literature NP219247.RAfNXP2SmjmGq1b8EXi-y0rYU07xGPmvxZ0o9kZDHe5uQ130_provenance.
- NP219247.RAfNXP2SmjmGq1b8EXi-y0rYU07xGPmvxZ0o9kZDHe5uQ130_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." NP219247.RAfNXP2SmjmGq1b8EXi-y0rYU07xGPmvxZ0o9kZDHe5uQ130_provenance.