Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP862653.RAdd053B0LBk2JGFYogNFdNY85AR8GMse6NE9Dt6pNEbI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP862653.RAdd053B0LBk2JGFYogNFdNY85AR8GMse6NE9Dt6pNEbI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP862653.RAdd053B0LBk2JGFYogNFdNY85AR8GMse6NE9Dt6pNEbI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP862653.RAdd053B0LBk2JGFYogNFdNY85AR8GMse6NE9Dt6pNEbI130_provenance.
- NP862653.RAdd053B0LBk2JGFYogNFdNY85AR8GMse6NE9Dt6pNEbI130_assertion description "[Since the incidence and clinical implications of abnormalities of TP53, CDKN2A (encoding for p16 and p14) and MDM2 genes (chromosome 12) in multiple myeloma (MM) is not clear, we investigated allelic loss at the former two loci and gain at the latter locus in a series of 82 MM patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP862653.RAdd053B0LBk2JGFYogNFdNY85AR8GMse6NE9Dt6pNEbI130_provenance.
- NP862653.RAdd053B0LBk2JGFYogNFdNY85AR8GMse6NE9Dt6pNEbI130_assertion evidence source_evidence_literature NP862653.RAdd053B0LBk2JGFYogNFdNY85AR8GMse6NE9Dt6pNEbI130_provenance.
- NP862653.RAdd053B0LBk2JGFYogNFdNY85AR8GMse6NE9Dt6pNEbI130_assertion SIO_000772 12745272 NP862653.RAdd053B0LBk2JGFYogNFdNY85AR8GMse6NE9Dt6pNEbI130_provenance.
- NP862653.RAdd053B0LBk2JGFYogNFdNY85AR8GMse6NE9Dt6pNEbI130_assertion wasDerivedFrom befree-20140225 NP862653.RAdd053B0LBk2JGFYogNFdNY85AR8GMse6NE9Dt6pNEbI130_provenance.
- NP862653.RAdd053B0LBk2JGFYogNFdNY85AR8GMse6NE9Dt6pNEbI130_assertion wasGeneratedBy ECO_0000203 NP862653.RAdd053B0LBk2JGFYogNFdNY85AR8GMse6NE9Dt6pNEbI130_provenance.
- befree-20140225 importedOn "2014-02-25" NP862653.RAdd053B0LBk2JGFYogNFdNY85AR8GMse6NE9Dt6pNEbI130_provenance.