Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP304248.RAuJe4mY_TCSDsNunX1c-_Po7kuzwCJU4F-xmZtf7kYrA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP304248.RAuJe4mY_TCSDsNunX1c-_Po7kuzwCJU4F-xmZtf7kYrA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP304248.RAuJe4mY_TCSDsNunX1c-_Po7kuzwCJU4F-xmZtf7kYrA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP304248.RAuJe4mY_TCSDsNunX1c-_Po7kuzwCJU4F-xmZtf7kYrA130_provenance.
- NP304248.RAuJe4mY_TCSDsNunX1c-_Po7kuzwCJU4F-xmZtf7kYrA130_assertion description "[In order to determine whether these genes are more widely involved in haematological malignancies, we have investigated a total of 84 samples that did not have homozygous p16 or p15 deletions from patients with acute lymphoid leukaemia (n=13), acute myeloid leukaemia (n=24) and chronic myeloid leukaemia in blast crisis (n=43) as well as four haemopoietic cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP304248.RAuJe4mY_TCSDsNunX1c-_Po7kuzwCJU4F-xmZtf7kYrA130_provenance.
- NP304248.RAuJe4mY_TCSDsNunX1c-_Po7kuzwCJU4F-xmZtf7kYrA130_assertion evidence source_evidence_literature NP304248.RAuJe4mY_TCSDsNunX1c-_Po7kuzwCJU4F-xmZtf7kYrA130_provenance.
- NP304248.RAuJe4mY_TCSDsNunX1c-_Po7kuzwCJU4F-xmZtf7kYrA130_assertion SIO_000772 8616035 NP304248.RAuJe4mY_TCSDsNunX1c-_Po7kuzwCJU4F-xmZtf7kYrA130_provenance.
- NP304248.RAuJe4mY_TCSDsNunX1c-_Po7kuzwCJU4F-xmZtf7kYrA130_assertion wasDerivedFrom befree-20150227 NP304248.RAuJe4mY_TCSDsNunX1c-_Po7kuzwCJU4F-xmZtf7kYrA130_provenance.
- NP304248.RAuJe4mY_TCSDsNunX1c-_Po7kuzwCJU4F-xmZtf7kYrA130_assertion wasGeneratedBy ECO_0000203 NP304248.RAuJe4mY_TCSDsNunX1c-_Po7kuzwCJU4F-xmZtf7kYrA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP304248.RAuJe4mY_TCSDsNunX1c-_Po7kuzwCJU4F-xmZtf7kYrA130_provenance.