Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP414767.RAHge8ZBIo8mzYj77Jav_eRRQFGx69TBEQNnsNSAk0moQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP414767.RAHge8ZBIo8mzYj77Jav_eRRQFGx69TBEQNnsNSAk0moQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP414767.RAHge8ZBIo8mzYj77Jav_eRRQFGx69TBEQNnsNSAk0moQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP414767.RAHge8ZBIo8mzYj77Jav_eRRQFGx69TBEQNnsNSAk0moQ130_provenance.
- NP414767.RAHge8ZBIo8mzYj77Jav_eRRQFGx69TBEQNnsNSAk0moQ130_assertion description "[Acquired mutations in GATA1 were detected in the vast majority of patients with acute megakaryoblastic leukemia (DS-AMKL) and in nearly every patient with transient myeloproliferative disorder (TMD), a preleukemia that may be present in as many as 10% of infants with DS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP414767.RAHge8ZBIo8mzYj77Jav_eRRQFGx69TBEQNnsNSAk0moQ130_provenance.
- NP414767.RAHge8ZBIo8mzYj77Jav_eRRQFGx69TBEQNnsNSAk0moQ130_assertion evidence source_evidence_literature NP414767.RAHge8ZBIo8mzYj77Jav_eRRQFGx69TBEQNnsNSAk0moQ130_provenance.
- NP414767.RAHge8ZBIo8mzYj77Jav_eRRQFGx69TBEQNnsNSAk0moQ130_assertion SIO_000772 14512321 NP414767.RAHge8ZBIo8mzYj77Jav_eRRQFGx69TBEQNnsNSAk0moQ130_provenance.
- NP414767.RAHge8ZBIo8mzYj77Jav_eRRQFGx69TBEQNnsNSAk0moQ130_assertion wasDerivedFrom befree-2016 NP414767.RAHge8ZBIo8mzYj77Jav_eRRQFGx69TBEQNnsNSAk0moQ130_provenance.
- NP414767.RAHge8ZBIo8mzYj77Jav_eRRQFGx69TBEQNnsNSAk0moQ130_assertion wasGeneratedBy ECO_0000203 NP414767.RAHge8ZBIo8mzYj77Jav_eRRQFGx69TBEQNnsNSAk0moQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP414767.RAHge8ZBIo8mzYj77Jav_eRRQFGx69TBEQNnsNSAk0moQ130_provenance.