Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP12639.RADY0uNH1xtlZoMyuGj7i2ACwpT4xmfyuc9BschTWtPAs130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP12639.RADY0uNH1xtlZoMyuGj7i2ACwpT4xmfyuc9BschTWtPAs130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP12639.RADY0uNH1xtlZoMyuGj7i2ACwpT4xmfyuc9BschTWtPAs130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP12639.RADY0uNH1xtlZoMyuGj7i2ACwpT4xmfyuc9BschTWtPAs130_provenance.
- NP12639.RADY0uNH1xtlZoMyuGj7i2ACwpT4xmfyuc9BschTWtPAs130_assertion description "[Functional impact of global rare copy number variation in autism spectrum disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP12639.RADY0uNH1xtlZoMyuGj7i2ACwpT4xmfyuc9BschTWtPAs130_provenance.
- NP12639.RADY0uNH1xtlZoMyuGj7i2ACwpT4xmfyuc9BschTWtPAs130_assertion evidence source_evidence_curated NP12639.RADY0uNH1xtlZoMyuGj7i2ACwpT4xmfyuc9BschTWtPAs130_provenance.
- NP12639.RADY0uNH1xtlZoMyuGj7i2ACwpT4xmfyuc9BschTWtPAs130_assertion SIO_000772 20531469 NP12639.RADY0uNH1xtlZoMyuGj7i2ACwpT4xmfyuc9BschTWtPAs130_provenance.
- NP12639.RADY0uNH1xtlZoMyuGj7i2ACwpT4xmfyuc9BschTWtPAs130_assertion wasDerivedFrom ctd_human-20150221 NP12639.RADY0uNH1xtlZoMyuGj7i2ACwpT4xmfyuc9BschTWtPAs130_provenance.
- NP12639.RADY0uNH1xtlZoMyuGj7i2ACwpT4xmfyuc9BschTWtPAs130_assertion wasGeneratedBy ECO_0000218 NP12639.RADY0uNH1xtlZoMyuGj7i2ACwpT4xmfyuc9BschTWtPAs130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP12639.RADY0uNH1xtlZoMyuGj7i2ACwpT4xmfyuc9BschTWtPAs130_provenance.