Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP307169.RAIIgAP9PEsUre29OCtgrOLnosaTqVkfJ8gIe5BTqY0GA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP307169.RAIIgAP9PEsUre29OCtgrOLnosaTqVkfJ8gIe5BTqY0GA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP307169.RAIIgAP9PEsUre29OCtgrOLnosaTqVkfJ8gIe5BTqY0GA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP307169.RAIIgAP9PEsUre29OCtgrOLnosaTqVkfJ8gIe5BTqY0GA130_provenance.
- NP307169.RAIIgAP9PEsUre29OCtgrOLnosaTqVkfJ8gIe5BTqY0GA130_assertion description "[These results revealed the frequent methylation of p16 and p15 genes in B-ALL and AML despite a low frequency of p16 and p15 deletions and mutations in these leukemias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307169.RAIIgAP9PEsUre29OCtgrOLnosaTqVkfJ8gIe5BTqY0GA130_provenance.
- NP307169.RAIIgAP9PEsUre29OCtgrOLnosaTqVkfJ8gIe5BTqY0GA130_assertion evidence source_evidence_literature NP307169.RAIIgAP9PEsUre29OCtgrOLnosaTqVkfJ8gIe5BTqY0GA130_provenance.
- NP307169.RAIIgAP9PEsUre29OCtgrOLnosaTqVkfJ8gIe5BTqY0GA130_assertion SIO_000772 10634644 NP307169.RAIIgAP9PEsUre29OCtgrOLnosaTqVkfJ8gIe5BTqY0GA130_provenance.
- NP307169.RAIIgAP9PEsUre29OCtgrOLnosaTqVkfJ8gIe5BTqY0GA130_assertion wasDerivedFrom befree-20150227 NP307169.RAIIgAP9PEsUre29OCtgrOLnosaTqVkfJ8gIe5BTqY0GA130_provenance.
- NP307169.RAIIgAP9PEsUre29OCtgrOLnosaTqVkfJ8gIe5BTqY0GA130_assertion wasGeneratedBy ECO_0000203 NP307169.RAIIgAP9PEsUre29OCtgrOLnosaTqVkfJ8gIe5BTqY0GA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP307169.RAIIgAP9PEsUre29OCtgrOLnosaTqVkfJ8gIe5BTqY0GA130_provenance.