Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP470562.RAQSRxlR2PwO8uIjwXHxOCrnLqsUxtwe9xLmjnafsgvmo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP470562.RAQSRxlR2PwO8uIjwXHxOCrnLqsUxtwe9xLmjnafsgvmo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP470562.RAQSRxlR2PwO8uIjwXHxOCrnLqsUxtwe9xLmjnafsgvmo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP470562.RAQSRxlR2PwO8uIjwXHxOCrnLqsUxtwe9xLmjnafsgvmo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP470562.RAQSRxlR2PwO8uIjwXHxOCrnLqsUxtwe9xLmjnafsgvmo130_provenance.
- NP470562.RAQSRxlR2PwO8uIjwXHxOCrnLqsUxtwe9xLmjnafsgvmo130_assertion wasGeneratedBy ECO_0000203 NP470562.RAQSRxlR2PwO8uIjwXHxOCrnLqsUxtwe9xLmjnafsgvmo130_provenance.
- NP470562.RAQSRxlR2PwO8uIjwXHxOCrnLqsUxtwe9xLmjnafsgvmo130_assertion wasDerivedFrom befree-20150227 NP470562.RAQSRxlR2PwO8uIjwXHxOCrnLqsUxtwe9xLmjnafsgvmo130_provenance.
- NP470562.RAQSRxlR2PwO8uIjwXHxOCrnLqsUxtwe9xLmjnafsgvmo130_assertion SIO_000772 22872102 NP470562.RAQSRxlR2PwO8uIjwXHxOCrnLqsUxtwe9xLmjnafsgvmo130_provenance.
- NP470562.RAQSRxlR2PwO8uIjwXHxOCrnLqsUxtwe9xLmjnafsgvmo130_assertion evidence source_evidence_literature NP470562.RAQSRxlR2PwO8uIjwXHxOCrnLqsUxtwe9xLmjnafsgvmo130_provenance.
- NP470562.RAQSRxlR2PwO8uIjwXHxOCrnLqsUxtwe9xLmjnafsgvmo130_assertion description "[Detection of copy-number variation in AUTS2 gene by targeted exonic array CGH in patients with developmental delay and autistic spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP470562.RAQSRxlR2PwO8uIjwXHxOCrnLqsUxtwe9xLmjnafsgvmo130_provenance.