Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1387823.RADog9MfBciysniNXh7X03l4tvaPlo0egLWa8yX1M9W1I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1387823.RADog9MfBciysniNXh7X03l4tvaPlo0egLWa8yX1M9W1I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1387823.RADog9MfBciysniNXh7X03l4tvaPlo0egLWa8yX1M9W1I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1387823.RADog9MfBciysniNXh7X03l4tvaPlo0egLWa8yX1M9W1I130_provenance.
- NP1387823.RADog9MfBciysniNXh7X03l4tvaPlo0egLWa8yX1M9W1I130_assertion description "[We identified homozygous deletion of p16 and p15 genes in five (19%) of 27 acute lymphoblastic leukemias (ALLs) and in two (11%) of 19 acute myeloid leukemias (AMLs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1387823.RADog9MfBciysniNXh7X03l4tvaPlo0egLWa8yX1M9W1I130_provenance.
- NP1387823.RADog9MfBciysniNXh7X03l4tvaPlo0egLWa8yX1M9W1I130_assertion evidence source_evidence_literature NP1387823.RADog9MfBciysniNXh7X03l4tvaPlo0egLWa8yX1M9W1I130_provenance.
- NP1387823.RADog9MfBciysniNXh7X03l4tvaPlo0egLWa8yX1M9W1I130_assertion SIO_000772 9447829 NP1387823.RADog9MfBciysniNXh7X03l4tvaPlo0egLWa8yX1M9W1I130_provenance.
- NP1387823.RADog9MfBciysniNXh7X03l4tvaPlo0egLWa8yX1M9W1I130_assertion wasDerivedFrom befree-2016 NP1387823.RADog9MfBciysniNXh7X03l4tvaPlo0egLWa8yX1M9W1I130_provenance.
- NP1387823.RADog9MfBciysniNXh7X03l4tvaPlo0egLWa8yX1M9W1I130_assertion wasGeneratedBy ECO_0000203 NP1387823.RADog9MfBciysniNXh7X03l4tvaPlo0egLWa8yX1M9W1I130_provenance.
- befree-2016 importedOn "2016-02-19" NP1387823.RADog9MfBciysniNXh7X03l4tvaPlo0egLWa8yX1M9W1I130_provenance.