Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP204903.RAJbHBuVoBcNiym_IhuA4asf5jwDkm3PEQc4TsyL5PFoE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP204903.RAJbHBuVoBcNiym_IhuA4asf5jwDkm3PEQc4TsyL5PFoE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP204903.RAJbHBuVoBcNiym_IhuA4asf5jwDkm3PEQc4TsyL5PFoE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP204903.RAJbHBuVoBcNiym_IhuA4asf5jwDkm3PEQc4TsyL5PFoE130_provenance.
- NP204903.RAJbHBuVoBcNiym_IhuA4asf5jwDkm3PEQc4TsyL5PFoE130_assertion description "[Selected candidate genes mapping within the aberrant genomic regions were sequenced and mutation of the TP53 gene was observed in one case in BC and of the ASXL1 gene in 6 of 41 cases in CP or BC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP204903.RAJbHBuVoBcNiym_IhuA4asf5jwDkm3PEQc4TsyL5PFoE130_provenance.
- NP204903.RAJbHBuVoBcNiym_IhuA4asf5jwDkm3PEQc4TsyL5PFoE130_assertion evidence source_evidence_literature NP204903.RAJbHBuVoBcNiym_IhuA4asf5jwDkm3PEQc4TsyL5PFoE130_provenance.
- NP204903.RAJbHBuVoBcNiym_IhuA4asf5jwDkm3PEQc4TsyL5PFoE130_assertion SIO_000772 20410925 NP204903.RAJbHBuVoBcNiym_IhuA4asf5jwDkm3PEQc4TsyL5PFoE130_provenance.
- NP204903.RAJbHBuVoBcNiym_IhuA4asf5jwDkm3PEQc4TsyL5PFoE130_assertion wasDerivedFrom befree-20140225 NP204903.RAJbHBuVoBcNiym_IhuA4asf5jwDkm3PEQc4TsyL5PFoE130_provenance.
- NP204903.RAJbHBuVoBcNiym_IhuA4asf5jwDkm3PEQc4TsyL5PFoE130_assertion wasGeneratedBy ECO_0000203 NP204903.RAJbHBuVoBcNiym_IhuA4asf5jwDkm3PEQc4TsyL5PFoE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP204903.RAJbHBuVoBcNiym_IhuA4asf5jwDkm3PEQc4TsyL5PFoE130_provenance.