Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1104476.RAm6lfz8IT_a3uNcDgFBJlG6wgyjeN-lDqjfLhRbIwcDQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1104476.RAm6lfz8IT_a3uNcDgFBJlG6wgyjeN-lDqjfLhRbIwcDQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1104476.RAm6lfz8IT_a3uNcDgFBJlG6wgyjeN-lDqjfLhRbIwcDQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1104476.RAm6lfz8IT_a3uNcDgFBJlG6wgyjeN-lDqjfLhRbIwcDQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1104476.RAm6lfz8IT_a3uNcDgFBJlG6wgyjeN-lDqjfLhRbIwcDQ130_provenance.
- NP1104476.RAm6lfz8IT_a3uNcDgFBJlG6wgyjeN-lDqjfLhRbIwcDQ130_assertion wasGeneratedBy ECO_0000203 NP1104476.RAm6lfz8IT_a3uNcDgFBJlG6wgyjeN-lDqjfLhRbIwcDQ130_provenance.
- NP1104476.RAm6lfz8IT_a3uNcDgFBJlG6wgyjeN-lDqjfLhRbIwcDQ130_assertion wasDerivedFrom befree-2016 NP1104476.RAm6lfz8IT_a3uNcDgFBJlG6wgyjeN-lDqjfLhRbIwcDQ130_provenance.
- NP1104476.RAm6lfz8IT_a3uNcDgFBJlG6wgyjeN-lDqjfLhRbIwcDQ130_assertion SIO_000772 23969274 NP1104476.RAm6lfz8IT_a3uNcDgFBJlG6wgyjeN-lDqjfLhRbIwcDQ130_provenance.
- NP1104476.RAm6lfz8IT_a3uNcDgFBJlG6wgyjeN-lDqjfLhRbIwcDQ130_assertion evidence source_evidence_literature NP1104476.RAm6lfz8IT_a3uNcDgFBJlG6wgyjeN-lDqjfLhRbIwcDQ130_provenance.
- NP1104476.RAm6lfz8IT_a3uNcDgFBJlG6wgyjeN-lDqjfLhRbIwcDQ130_assertion description "[To evaluate the role of whole genome comparative genomic hybridisation microarray (array-CGH) in detecting genomic imbalances as compared to conventional karyotype (GTG-analysis) or myeloma specific fluorescence in situ hybridisation (FISH) panel in a diagnostic setting for plasma cell dyscrasia (PCD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1104476.RAm6lfz8IT_a3uNcDgFBJlG6wgyjeN-lDqjfLhRbIwcDQ130_provenance.