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- source_evidence_literature type ECO_0000212 NP1003491.RAMDqusEZZ5WAcTbPcnv8kTPwZCL45_bcWRz-hkSpeTeE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1003491.RAMDqusEZZ5WAcTbPcnv8kTPwZCL45_bcWRz-hkSpeTeE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1003491.RAMDqusEZZ5WAcTbPcnv8kTPwZCL45_bcWRz-hkSpeTeE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1003491.RAMDqusEZZ5WAcTbPcnv8kTPwZCL45_bcWRz-hkSpeTeE130_provenance.
- NP1003491.RAMDqusEZZ5WAcTbPcnv8kTPwZCL45_bcWRz-hkSpeTeE130_assertion wasGeneratedBy ECO_0000203 NP1003491.RAMDqusEZZ5WAcTbPcnv8kTPwZCL45_bcWRz-hkSpeTeE130_provenance.
- NP1003491.RAMDqusEZZ5WAcTbPcnv8kTPwZCL45_bcWRz-hkSpeTeE130_assertion wasDerivedFrom befree-2016 NP1003491.RAMDqusEZZ5WAcTbPcnv8kTPwZCL45_bcWRz-hkSpeTeE130_provenance.
- NP1003491.RAMDqusEZZ5WAcTbPcnv8kTPwZCL45_bcWRz-hkSpeTeE130_assertion SIO_000772 22872102 NP1003491.RAMDqusEZZ5WAcTbPcnv8kTPwZCL45_bcWRz-hkSpeTeE130_provenance.
- NP1003491.RAMDqusEZZ5WAcTbPcnv8kTPwZCL45_bcWRz-hkSpeTeE130_assertion evidence source_evidence_literature NP1003491.RAMDqusEZZ5WAcTbPcnv8kTPwZCL45_bcWRz-hkSpeTeE130_provenance.
- NP1003491.RAMDqusEZZ5WAcTbPcnv8kTPwZCL45_bcWRz-hkSpeTeE130_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." NP1003491.RAMDqusEZZ5WAcTbPcnv8kTPwZCL45_bcWRz-hkSpeTeE130_provenance.