Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP516682.RAKMWTFSFQtCrpBsZbVFqs3febP4Nh0t-FQI_QFFynLOs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP516682.RAKMWTFSFQtCrpBsZbVFqs3febP4Nh0t-FQI_QFFynLOs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP516682.RAKMWTFSFQtCrpBsZbVFqs3febP4Nh0t-FQI_QFFynLOs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP516682.RAKMWTFSFQtCrpBsZbVFqs3febP4Nh0t-FQI_QFFynLOs130_provenance.
- NP516682.RAKMWTFSFQtCrpBsZbVFqs3febP4Nh0t-FQI_QFFynLOs130_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." NP516682.RAKMWTFSFQtCrpBsZbVFqs3febP4Nh0t-FQI_QFFynLOs130_provenance.
- NP516682.RAKMWTFSFQtCrpBsZbVFqs3febP4Nh0t-FQI_QFFynLOs130_assertion evidence source_evidence_literature NP516682.RAKMWTFSFQtCrpBsZbVFqs3febP4Nh0t-FQI_QFFynLOs130_provenance.
- NP516682.RAKMWTFSFQtCrpBsZbVFqs3febP4Nh0t-FQI_QFFynLOs130_assertion SIO_000772 10498868 NP516682.RAKMWTFSFQtCrpBsZbVFqs3febP4Nh0t-FQI_QFFynLOs130_provenance.
- NP516682.RAKMWTFSFQtCrpBsZbVFqs3febP4Nh0t-FQI_QFFynLOs130_assertion wasDerivedFrom befree-20140225 NP516682.RAKMWTFSFQtCrpBsZbVFqs3febP4Nh0t-FQI_QFFynLOs130_provenance.
- NP516682.RAKMWTFSFQtCrpBsZbVFqs3febP4Nh0t-FQI_QFFynLOs130_assertion wasGeneratedBy ECO_0000203 NP516682.RAKMWTFSFQtCrpBsZbVFqs3febP4Nh0t-FQI_QFFynLOs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP516682.RAKMWTFSFQtCrpBsZbVFqs3febP4Nh0t-FQI_QFFynLOs130_provenance.