Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP263971.RAU4Q0YRafiVeoVhsTqzKqdBYZY0ZNcWLnI_YDgSbU4_k130_assertion> ?p ?o ?g. }
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- NP263971.RAU4Q0YRafiVeoVhsTqzKqdBYZY0ZNcWLnI_YDgSbU4_k130_assertion type Assertion NP263971.RAU4Q0YRafiVeoVhsTqzKqdBYZY0ZNcWLnI_YDgSbU4_k130_head.
- 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.