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- source_evidence_literature type ECO_0000212 NP694557.RALmunBU5fRDIRf42NgERdmQYkDEE27D-mpj49kGuPgh8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694557.RALmunBU5fRDIRf42NgERdmQYkDEE27D-mpj49kGuPgh8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694557.RALmunBU5fRDIRf42NgERdmQYkDEE27D-mpj49kGuPgh8130_provenance.
- NP694557.RALmunBU5fRDIRf42NgERdmQYkDEE27D-mpj49kGuPgh8130_assertion description "[Our findings demonstrate a novel genomic disorder characterised by deletion of BMP2 with variable cognitive deficits and dysmorphic features and show that individuals bearing microdeletions in 20p12.3 often present with WPW syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694557.RALmunBU5fRDIRf42NgERdmQYkDEE27D-mpj49kGuPgh8130_provenance.
- NP694557.RALmunBU5fRDIRf42NgERdmQYkDEE27D-mpj49kGuPgh8130_assertion evidence source_evidence_literature NP694557.RALmunBU5fRDIRf42NgERdmQYkDEE27D-mpj49kGuPgh8130_provenance.
- NP694557.RALmunBU5fRDIRf42NgERdmQYkDEE27D-mpj49kGuPgh8130_assertion SIO_000772 18812404 NP694557.RALmunBU5fRDIRf42NgERdmQYkDEE27D-mpj49kGuPgh8130_provenance.
- NP694557.RALmunBU5fRDIRf42NgERdmQYkDEE27D-mpj49kGuPgh8130_assertion wasDerivedFrom befree-2016 NP694557.RALmunBU5fRDIRf42NgERdmQYkDEE27D-mpj49kGuPgh8130_provenance.
- NP694557.RALmunBU5fRDIRf42NgERdmQYkDEE27D-mpj49kGuPgh8130_assertion wasGeneratedBy ECO_0000203 NP694557.RALmunBU5fRDIRf42NgERdmQYkDEE27D-mpj49kGuPgh8130_provenance.
- befree-2016 importedOn "2016-02-19" NP694557.RALmunBU5fRDIRf42NgERdmQYkDEE27D-mpj49kGuPgh8130_provenance.