Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP285519.RAeOaMFthb-Z5YKTQwYlh_lEbB_ijGPyKrMgAgPYB6RwI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP285519.RAeOaMFthb-Z5YKTQwYlh_lEbB_ijGPyKrMgAgPYB6RwI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285519.RAeOaMFthb-Z5YKTQwYlh_lEbB_ijGPyKrMgAgPYB6RwI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285519.RAeOaMFthb-Z5YKTQwYlh_lEbB_ijGPyKrMgAgPYB6RwI130_provenance.
- NP285519.RAeOaMFthb-Z5YKTQwYlh_lEbB_ijGPyKrMgAgPYB6RwI130_assertion description "[The t(8;21) RUNX1-ETO translocation is one of the most frequent cytogenetic abnormalities in acute myeloid leukemia (AML).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285519.RAeOaMFthb-Z5YKTQwYlh_lEbB_ijGPyKrMgAgPYB6RwI130_provenance.
- NP285519.RAeOaMFthb-Z5YKTQwYlh_lEbB_ijGPyKrMgAgPYB6RwI130_assertion evidence source_evidence_literature NP285519.RAeOaMFthb-Z5YKTQwYlh_lEbB_ijGPyKrMgAgPYB6RwI130_provenance.
- NP285519.RAeOaMFthb-Z5YKTQwYlh_lEbB_ijGPyKrMgAgPYB6RwI130_assertion SIO_000772 21937700 NP285519.RAeOaMFthb-Z5YKTQwYlh_lEbB_ijGPyKrMgAgPYB6RwI130_provenance.
- NP285519.RAeOaMFthb-Z5YKTQwYlh_lEbB_ijGPyKrMgAgPYB6RwI130_assertion wasDerivedFrom befree-20150227 NP285519.RAeOaMFthb-Z5YKTQwYlh_lEbB_ijGPyKrMgAgPYB6RwI130_provenance.
- NP285519.RAeOaMFthb-Z5YKTQwYlh_lEbB_ijGPyKrMgAgPYB6RwI130_assertion wasGeneratedBy ECO_0000203 NP285519.RAeOaMFthb-Z5YKTQwYlh_lEbB_ijGPyKrMgAgPYB6RwI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP285519.RAeOaMFthb-Z5YKTQwYlh_lEbB_ijGPyKrMgAgPYB6RwI130_provenance.