Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP509791.RAjDNrVQ1YgDEKA7yojd__fdI6N_RbNs45XtLfuaseJZY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP509791.RAjDNrVQ1YgDEKA7yojd__fdI6N_RbNs45XtLfuaseJZY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP509791.RAjDNrVQ1YgDEKA7yojd__fdI6N_RbNs45XtLfuaseJZY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP509791.RAjDNrVQ1YgDEKA7yojd__fdI6N_RbNs45XtLfuaseJZY130_provenance.
- NP509791.RAjDNrVQ1YgDEKA7yojd__fdI6N_RbNs45XtLfuaseJZY130_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." NP509791.RAjDNrVQ1YgDEKA7yojd__fdI6N_RbNs45XtLfuaseJZY130_provenance.
- NP509791.RAjDNrVQ1YgDEKA7yojd__fdI6N_RbNs45XtLfuaseJZY130_assertion evidence source_evidence_literature NP509791.RAjDNrVQ1YgDEKA7yojd__fdI6N_RbNs45XtLfuaseJZY130_provenance.
- NP509791.RAjDNrVQ1YgDEKA7yojd__fdI6N_RbNs45XtLfuaseJZY130_assertion SIO_000772 10498868 NP509791.RAjDNrVQ1YgDEKA7yojd__fdI6N_RbNs45XtLfuaseJZY130_provenance.
- NP509791.RAjDNrVQ1YgDEKA7yojd__fdI6N_RbNs45XtLfuaseJZY130_assertion wasDerivedFrom befree-20150227 NP509791.RAjDNrVQ1YgDEKA7yojd__fdI6N_RbNs45XtLfuaseJZY130_provenance.
- NP509791.RAjDNrVQ1YgDEKA7yojd__fdI6N_RbNs45XtLfuaseJZY130_assertion wasGeneratedBy ECO_0000203 NP509791.RAjDNrVQ1YgDEKA7yojd__fdI6N_RbNs45XtLfuaseJZY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP509791.RAjDNrVQ1YgDEKA7yojd__fdI6N_RbNs45XtLfuaseJZY130_provenance.