Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1312134.RAhmDEWNHHlI1_0RpSeMcmFM2VlW05E5EJzqWcRoSwJtE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1312134.RAhmDEWNHHlI1_0RpSeMcmFM2VlW05E5EJzqWcRoSwJtE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1312134.RAhmDEWNHHlI1_0RpSeMcmFM2VlW05E5EJzqWcRoSwJtE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1312134.RAhmDEWNHHlI1_0RpSeMcmFM2VlW05E5EJzqWcRoSwJtE130_provenance.
- NP1312134.RAhmDEWNHHlI1_0RpSeMcmFM2VlW05E5EJzqWcRoSwJtE130_assertion description "[The human tri-thorax gene (HRX) also called ALL-1 (Acute Lymphocytic Leukemia-1) as well as MLL (Myeloid-lymphoid or Mixed-lineage Leukemia) gene, is disrupted in the majority of leukemias with chromosomal abnormalities involving 11q23.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1312134.RAhmDEWNHHlI1_0RpSeMcmFM2VlW05E5EJzqWcRoSwJtE130_provenance.
- NP1312134.RAhmDEWNHHlI1_0RpSeMcmFM2VlW05E5EJzqWcRoSwJtE130_assertion evidence source_evidence_literature NP1312134.RAhmDEWNHHlI1_0RpSeMcmFM2VlW05E5EJzqWcRoSwJtE130_provenance.
- NP1312134.RAhmDEWNHHlI1_0RpSeMcmFM2VlW05E5EJzqWcRoSwJtE130_assertion SIO_000772 7549829 NP1312134.RAhmDEWNHHlI1_0RpSeMcmFM2VlW05E5EJzqWcRoSwJtE130_provenance.
- NP1312134.RAhmDEWNHHlI1_0RpSeMcmFM2VlW05E5EJzqWcRoSwJtE130_assertion wasDerivedFrom befree-2016 NP1312134.RAhmDEWNHHlI1_0RpSeMcmFM2VlW05E5EJzqWcRoSwJtE130_provenance.
- NP1312134.RAhmDEWNHHlI1_0RpSeMcmFM2VlW05E5EJzqWcRoSwJtE130_assertion wasGeneratedBy ECO_0000203 NP1312134.RAhmDEWNHHlI1_0RpSeMcmFM2VlW05E5EJzqWcRoSwJtE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1312134.RAhmDEWNHHlI1_0RpSeMcmFM2VlW05E5EJzqWcRoSwJtE130_provenance.