Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP898259.RAUj1eoOAEdj_b_efIa5DMMtZHQ8SKhkgovTzH1adYgN8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP898259.RAUj1eoOAEdj_b_efIa5DMMtZHQ8SKhkgovTzH1adYgN8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP898259.RAUj1eoOAEdj_b_efIa5DMMtZHQ8SKhkgovTzH1adYgN8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP898259.RAUj1eoOAEdj_b_efIa5DMMtZHQ8SKhkgovTzH1adYgN8130_provenance.
- befree-2016 importedOn "2016-02-19" NP898259.RAUj1eoOAEdj_b_efIa5DMMtZHQ8SKhkgovTzH1adYgN8130_provenance.
- NP898259.RAUj1eoOAEdj_b_efIa5DMMtZHQ8SKhkgovTzH1adYgN8130_assertion wasGeneratedBy ECO_0000203 NP898259.RAUj1eoOAEdj_b_efIa5DMMtZHQ8SKhkgovTzH1adYgN8130_provenance.
- NP898259.RAUj1eoOAEdj_b_efIa5DMMtZHQ8SKhkgovTzH1adYgN8130_assertion wasDerivedFrom befree-2016 NP898259.RAUj1eoOAEdj_b_efIa5DMMtZHQ8SKhkgovTzH1adYgN8130_provenance.
- NP898259.RAUj1eoOAEdj_b_efIa5DMMtZHQ8SKhkgovTzH1adYgN8130_assertion SIO_000772 21627674 NP898259.RAUj1eoOAEdj_b_efIa5DMMtZHQ8SKhkgovTzH1adYgN8130_provenance.
- NP898259.RAUj1eoOAEdj_b_efIa5DMMtZHQ8SKhkgovTzH1adYgN8130_assertion evidence source_evidence_literature NP898259.RAUj1eoOAEdj_b_efIa5DMMtZHQ8SKhkgovTzH1adYgN8130_provenance.
- NP898259.RAUj1eoOAEdj_b_efIa5DMMtZHQ8SKhkgovTzH1adYgN8130_assertion description "[Although large MEN1 deletion causes MEN1, disruption of imprinted CDKN1C/p57KIP2 and IGF-2 gene expression may contribute to tumour progression and aggressive phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898259.RAUj1eoOAEdj_b_efIa5DMMtZHQ8SKhkgovTzH1adYgN8130_provenance.