Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP470724.RAUO8iHWXWvmkBaV9ua_El8P_sY2XS3k63ZzZBLA0G-7U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP470724.RAUO8iHWXWvmkBaV9ua_El8P_sY2XS3k63ZzZBLA0G-7U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470724.RAUO8iHWXWvmkBaV9ua_El8P_sY2XS3k63ZzZBLA0G-7U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470724.RAUO8iHWXWvmkBaV9ua_El8P_sY2XS3k63ZzZBLA0G-7U130_provenance.
- NP470724.RAUO8iHWXWvmkBaV9ua_El8P_sY2XS3k63ZzZBLA0G-7U130_assertion description "[The rationale of this array-CGH study was to characterize copy number imbalances of chromosome 1 in meningioma, using a full-coverage genomic microarray containing 2,118 distinct measurement points.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470724.RAUO8iHWXWvmkBaV9ua_El8P_sY2XS3k63ZzZBLA0G-7U130_provenance.
- NP470724.RAUO8iHWXWvmkBaV9ua_El8P_sY2XS3k63ZzZBLA0G-7U130_assertion evidence source_evidence_literature NP470724.RAUO8iHWXWvmkBaV9ua_El8P_sY2XS3k63ZzZBLA0G-7U130_provenance.
- NP470724.RAUO8iHWXWvmkBaV9ua_El8P_sY2XS3k63ZzZBLA0G-7U130_assertion SIO_000772 15805262 NP470724.RAUO8iHWXWvmkBaV9ua_El8P_sY2XS3k63ZzZBLA0G-7U130_provenance.
- NP470724.RAUO8iHWXWvmkBaV9ua_El8P_sY2XS3k63ZzZBLA0G-7U130_assertion wasDerivedFrom befree-20150227 NP470724.RAUO8iHWXWvmkBaV9ua_El8P_sY2XS3k63ZzZBLA0G-7U130_provenance.
- NP470724.RAUO8iHWXWvmkBaV9ua_El8P_sY2XS3k63ZzZBLA0G-7U130_assertion wasGeneratedBy ECO_0000203 NP470724.RAUO8iHWXWvmkBaV9ua_El8P_sY2XS3k63ZzZBLA0G-7U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP470724.RAUO8iHWXWvmkBaV9ua_El8P_sY2XS3k63ZzZBLA0G-7U130_provenance.