Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP470224.RAai1Pk-SnmT8z0LJTL1kFSCSFAv3VEa-IRKUU7B9Ndzk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP470224.RAai1Pk-SnmT8z0LJTL1kFSCSFAv3VEa-IRKUU7B9Ndzk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470224.RAai1Pk-SnmT8z0LJTL1kFSCSFAv3VEa-IRKUU7B9Ndzk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470224.RAai1Pk-SnmT8z0LJTL1kFSCSFAv3VEa-IRKUU7B9Ndzk130_provenance.
- NP470224.RAai1Pk-SnmT8z0LJTL1kFSCSFAv3VEa-IRKUU7B9Ndzk130_assertion description "[We have explored the application of array-CGH to the detection of such changes on a set of 20 samples consisting of patients with eye diseases associated with changes on chromosome 6p25 together with unaffected individuals, as well as two samples from tuberous sclerosis 2 (TSC2)-affected patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470224.RAai1Pk-SnmT8z0LJTL1kFSCSFAv3VEa-IRKUU7B9Ndzk130_provenance.
- NP470224.RAai1Pk-SnmT8z0LJTL1kFSCSFAv3VEa-IRKUU7B9Ndzk130_assertion evidence source_evidence_literature NP470224.RAai1Pk-SnmT8z0LJTL1kFSCSFAv3VEa-IRKUU7B9Ndzk130_provenance.
- NP470224.RAai1Pk-SnmT8z0LJTL1kFSCSFAv3VEa-IRKUU7B9Ndzk130_assertion SIO_000772 15221791 NP470224.RAai1Pk-SnmT8z0LJTL1kFSCSFAv3VEa-IRKUU7B9Ndzk130_provenance.
- NP470224.RAai1Pk-SnmT8z0LJTL1kFSCSFAv3VEa-IRKUU7B9Ndzk130_assertion wasDerivedFrom befree-20150227 NP470224.RAai1Pk-SnmT8z0LJTL1kFSCSFAv3VEa-IRKUU7B9Ndzk130_provenance.
- NP470224.RAai1Pk-SnmT8z0LJTL1kFSCSFAv3VEa-IRKUU7B9Ndzk130_assertion wasGeneratedBy ECO_0000203 NP470224.RAai1Pk-SnmT8z0LJTL1kFSCSFAv3VEa-IRKUU7B9Ndzk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP470224.RAai1Pk-SnmT8z0LJTL1kFSCSFAv3VEa-IRKUU7B9Ndzk130_provenance.