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- source_evidence_literature type ECO_0000212 NP263971.RAU4Q0YRafiVeoVhsTqzKqdBYZY0ZNcWLnI_YDgSbU4_k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP263971.RAU4Q0YRafiVeoVhsTqzKqdBYZY0ZNcWLnI_YDgSbU4_k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP263971.RAU4Q0YRafiVeoVhsTqzKqdBYZY0ZNcWLnI_YDgSbU4_k130_provenance.
- NP263971.RAU4Q0YRafiVeoVhsTqzKqdBYZY0ZNcWLnI_YDgSbU4_k130_assertion description "[Thus, ING1 mutation is very rare in breast or ovarian cancers, however, repression of ING1 expression frequently accompanies tumour development of breast cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263971.RAU4Q0YRafiVeoVhsTqzKqdBYZY0ZNcWLnI_YDgSbU4_k130_provenance.
- NP263971.RAU4Q0YRafiVeoVhsTqzKqdBYZY0ZNcWLnI_YDgSbU4_k130_assertion evidence source_evidence_literature NP263971.RAU4Q0YRafiVeoVhsTqzKqdBYZY0ZNcWLnI_YDgSbU4_k130_provenance.
- NP263971.RAU4Q0YRafiVeoVhsTqzKqdBYZY0ZNcWLnI_YDgSbU4_k130_assertion SIO_000772 10498868 NP263971.RAU4Q0YRafiVeoVhsTqzKqdBYZY0ZNcWLnI_YDgSbU4_k130_provenance.
- NP263971.RAU4Q0YRafiVeoVhsTqzKqdBYZY0ZNcWLnI_YDgSbU4_k130_assertion wasDerivedFrom befree-2016 NP263971.RAU4Q0YRafiVeoVhsTqzKqdBYZY0ZNcWLnI_YDgSbU4_k130_provenance.
- NP263971.RAU4Q0YRafiVeoVhsTqzKqdBYZY0ZNcWLnI_YDgSbU4_k130_assertion wasGeneratedBy ECO_0000203 NP263971.RAU4Q0YRafiVeoVhsTqzKqdBYZY0ZNcWLnI_YDgSbU4_k130_provenance.
- befree-2016 importedOn "2016-02-19" NP263971.RAU4Q0YRafiVeoVhsTqzKqdBYZY0ZNcWLnI_YDgSbU4_k130_provenance.