Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP867222.RAXqe0ryjemveA9zQbTsAk-a3D7sRgfdmI03K5J4NMKp0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP867222.RAXqe0ryjemveA9zQbTsAk-a3D7sRgfdmI03K5J4NMKp0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP867222.RAXqe0ryjemveA9zQbTsAk-a3D7sRgfdmI03K5J4NMKp0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP867222.RAXqe0ryjemveA9zQbTsAk-a3D7sRgfdmI03K5J4NMKp0130_provenance.
- NP867222.RAXqe0ryjemveA9zQbTsAk-a3D7sRgfdmI03K5J4NMKp0130_assertion description "[The phenotype HP1 was found to have an increased incidence in the total patient group due to an increased incidence in those with AML, ALL and CML compared with controls, but not in those with CLL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP867222.RAXqe0ryjemveA9zQbTsAk-a3D7sRgfdmI03K5J4NMKp0130_provenance.
- NP867222.RAXqe0ryjemveA9zQbTsAk-a3D7sRgfdmI03K5J4NMKp0130_assertion evidence source_evidence_literature NP867222.RAXqe0ryjemveA9zQbTsAk-a3D7sRgfdmI03K5J4NMKp0130_provenance.
- NP867222.RAXqe0ryjemveA9zQbTsAk-a3D7sRgfdmI03K5J4NMKp0130_assertion SIO_000772 3397067 NP867222.RAXqe0ryjemveA9zQbTsAk-a3D7sRgfdmI03K5J4NMKp0130_provenance.
- NP867222.RAXqe0ryjemveA9zQbTsAk-a3D7sRgfdmI03K5J4NMKp0130_assertion wasDerivedFrom befree-20140225 NP867222.RAXqe0ryjemveA9zQbTsAk-a3D7sRgfdmI03K5J4NMKp0130_provenance.
- NP867222.RAXqe0ryjemveA9zQbTsAk-a3D7sRgfdmI03K5J4NMKp0130_assertion wasGeneratedBy ECO_0000203 NP867222.RAXqe0ryjemveA9zQbTsAk-a3D7sRgfdmI03K5J4NMKp0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP867222.RAXqe0ryjemveA9zQbTsAk-a3D7sRgfdmI03K5J4NMKp0130_provenance.