Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668281.RAdFA-Vfih1Fk3rHdp24fpR32GVuzZH5oNrVj25swydGs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP668281.RAdFA-Vfih1Fk3rHdp24fpR32GVuzZH5oNrVj25swydGs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668281.RAdFA-Vfih1Fk3rHdp24fpR32GVuzZH5oNrVj25swydGs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668281.RAdFA-Vfih1Fk3rHdp24fpR32GVuzZH5oNrVj25swydGs130_provenance.
- NP668281.RAdFA-Vfih1Fk3rHdp24fpR32GVuzZH5oNrVj25swydGs130_assertion description "[The analysis of the p53 mutational spectrum in human cancers has provided evidence that both exogenous and endogenous causes of mutation contribute to human carcinogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668281.RAdFA-Vfih1Fk3rHdp24fpR32GVuzZH5oNrVj25swydGs130_provenance.
- NP668281.RAdFA-Vfih1Fk3rHdp24fpR32GVuzZH5oNrVj25swydGs130_assertion evidence source_evidence_literature NP668281.RAdFA-Vfih1Fk3rHdp24fpR32GVuzZH5oNrVj25swydGs130_provenance.
- NP668281.RAdFA-Vfih1Fk3rHdp24fpR32GVuzZH5oNrVj25swydGs130_assertion SIO_000772 1844248 NP668281.RAdFA-Vfih1Fk3rHdp24fpR32GVuzZH5oNrVj25swydGs130_provenance.
- NP668281.RAdFA-Vfih1Fk3rHdp24fpR32GVuzZH5oNrVj25swydGs130_assertion wasDerivedFrom befree-2016 NP668281.RAdFA-Vfih1Fk3rHdp24fpR32GVuzZH5oNrVj25swydGs130_provenance.
- NP668281.RAdFA-Vfih1Fk3rHdp24fpR32GVuzZH5oNrVj25swydGs130_assertion wasGeneratedBy ECO_0000203 NP668281.RAdFA-Vfih1Fk3rHdp24fpR32GVuzZH5oNrVj25swydGs130_provenance.
- befree-2016 importedOn "2016-02-19" NP668281.RAdFA-Vfih1Fk3rHdp24fpR32GVuzZH5oNrVj25swydGs130_provenance.