Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1348343.RAr0W55ryCiK0d39DLNmRLs1Sv2m8IIQe7xRFeY1J7Nc4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1348343.RAr0W55ryCiK0d39DLNmRLs1Sv2m8IIQe7xRFeY1J7Nc4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1348343.RAr0W55ryCiK0d39DLNmRLs1Sv2m8IIQe7xRFeY1J7Nc4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1348343.RAr0W55ryCiK0d39DLNmRLs1Sv2m8IIQe7xRFeY1J7Nc4130_provenance.
- NP1348343.RAr0W55ryCiK0d39DLNmRLs1Sv2m8IIQe7xRFeY1J7Nc4130_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." NP1348343.RAr0W55ryCiK0d39DLNmRLs1Sv2m8IIQe7xRFeY1J7Nc4130_provenance.
- NP1348343.RAr0W55ryCiK0d39DLNmRLs1Sv2m8IIQe7xRFeY1J7Nc4130_assertion evidence source_evidence_literature NP1348343.RAr0W55ryCiK0d39DLNmRLs1Sv2m8IIQe7xRFeY1J7Nc4130_provenance.
- NP1348343.RAr0W55ryCiK0d39DLNmRLs1Sv2m8IIQe7xRFeY1J7Nc4130_assertion SIO_000772 8616035 NP1348343.RAr0W55ryCiK0d39DLNmRLs1Sv2m8IIQe7xRFeY1J7Nc4130_provenance.
- NP1348343.RAr0W55ryCiK0d39DLNmRLs1Sv2m8IIQe7xRFeY1J7Nc4130_assertion wasDerivedFrom befree-2016 NP1348343.RAr0W55ryCiK0d39DLNmRLs1Sv2m8IIQe7xRFeY1J7Nc4130_provenance.
- NP1348343.RAr0W55ryCiK0d39DLNmRLs1Sv2m8IIQe7xRFeY1J7Nc4130_assertion wasGeneratedBy ECO_0000203 NP1348343.RAr0W55ryCiK0d39DLNmRLs1Sv2m8IIQe7xRFeY1J7Nc4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1348343.RAr0W55ryCiK0d39DLNmRLs1Sv2m8IIQe7xRFeY1J7Nc4130_provenance.