Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP702573.RAiEByPqLnyyAQ_tijnfepP4sQKvXY3JYGewyYwpPV9K0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP702573.RAiEByPqLnyyAQ_tijnfepP4sQKvXY3JYGewyYwpPV9K0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP702573.RAiEByPqLnyyAQ_tijnfepP4sQKvXY3JYGewyYwpPV9K0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP702573.RAiEByPqLnyyAQ_tijnfepP4sQKvXY3JYGewyYwpPV9K0130_provenance.
- NP702573.RAiEByPqLnyyAQ_tijnfepP4sQKvXY3JYGewyYwpPV9K0130_assertion description "[RUNX1 gene alterations are associated with acquired and inherited hematologic malignancies that include familial platelet disorder/acute myeloid leukemia, primary or secondary acute myeloid leukemia, and chronic myelomonocytic leukemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP702573.RAiEByPqLnyyAQ_tijnfepP4sQKvXY3JYGewyYwpPV9K0130_provenance.
- NP702573.RAiEByPqLnyyAQ_tijnfepP4sQKvXY3JYGewyYwpPV9K0130_assertion evidence source_evidence_literature NP702573.RAiEByPqLnyyAQ_tijnfepP4sQKvXY3JYGewyYwpPV9K0130_provenance.
- NP702573.RAiEByPqLnyyAQ_tijnfepP4sQKvXY3JYGewyYwpPV9K0130_assertion SIO_000772 22677128 NP702573.RAiEByPqLnyyAQ_tijnfepP4sQKvXY3JYGewyYwpPV9K0130_provenance.
- NP702573.RAiEByPqLnyyAQ_tijnfepP4sQKvXY3JYGewyYwpPV9K0130_assertion wasDerivedFrom befree-20140225 NP702573.RAiEByPqLnyyAQ_tijnfepP4sQKvXY3JYGewyYwpPV9K0130_provenance.
- NP702573.RAiEByPqLnyyAQ_tijnfepP4sQKvXY3JYGewyYwpPV9K0130_assertion wasGeneratedBy ECO_0000203 NP702573.RAiEByPqLnyyAQ_tijnfepP4sQKvXY3JYGewyYwpPV9K0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP702573.RAiEByPqLnyyAQ_tijnfepP4sQKvXY3JYGewyYwpPV9K0130_provenance.