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- source_evidence_literature type ECO_0000212 NP1029704.RAB2b_058H_WWceMlc_nSb-8oTHff93SRrcu4Bp1bKsn0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1029704.RAB2b_058H_WWceMlc_nSb-8oTHff93SRrcu4Bp1bKsn0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1029704.RAB2b_058H_WWceMlc_nSb-8oTHff93SRrcu4Bp1bKsn0130_provenance.
- NP1029704.RAB2b_058H_WWceMlc_nSb-8oTHff93SRrcu4Bp1bKsn0130_assertion description "[Array comparative genomic hybridization (CGH) demonstrated a 1.5-Mb terminal deletion of the long arm of chromosome 20, which included deletion of the KCNQ2 and CHRNA4 genes, both of which have been associated with specific epilepsy syndromes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1029704.RAB2b_058H_WWceMlc_nSb-8oTHff93SRrcu4Bp1bKsn0130_provenance.
- NP1029704.RAB2b_058H_WWceMlc_nSb-8oTHff93SRrcu4Bp1bKsn0130_assertion evidence source_evidence_literature NP1029704.RAB2b_058H_WWceMlc_nSb-8oTHff93SRrcu4Bp1bKsn0130_provenance.
- NP1029704.RAB2b_058H_WWceMlc_nSb-8oTHff93SRrcu4Bp1bKsn0130_assertion SIO_000772 23166088 NP1029704.RAB2b_058H_WWceMlc_nSb-8oTHff93SRrcu4Bp1bKsn0130_provenance.
- NP1029704.RAB2b_058H_WWceMlc_nSb-8oTHff93SRrcu4Bp1bKsn0130_assertion wasDerivedFrom befree-2016 NP1029704.RAB2b_058H_WWceMlc_nSb-8oTHff93SRrcu4Bp1bKsn0130_provenance.
- NP1029704.RAB2b_058H_WWceMlc_nSb-8oTHff93SRrcu4Bp1bKsn0130_assertion wasGeneratedBy ECO_0000203 NP1029704.RAB2b_058H_WWceMlc_nSb-8oTHff93SRrcu4Bp1bKsn0130_provenance.
- befree-2016 importedOn "2016-02-19" NP1029704.RAB2b_058H_WWceMlc_nSb-8oTHff93SRrcu4Bp1bKsn0130_provenance.