Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP702.RAAaoULVMWYcFbjFLtwiCZUktF2pdjwDOv6zf0qiCl3t0130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP702.RAAaoULVMWYcFbjFLtwiCZUktF2pdjwDOv6zf0qiCl3t0130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP702.RAAaoULVMWYcFbjFLtwiCZUktF2pdjwDOv6zf0qiCl3t0130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP702.RAAaoULVMWYcFbjFLtwiCZUktF2pdjwDOv6zf0qiCl3t0130_provenance.
- NP702.RAAaoULVMWYcFbjFLtwiCZUktF2pdjwDOv6zf0qiCl3t0130_assertion description "[Identification of a novel missense mutation of the SMN(T) gene in two siblings with spinal muscular atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP702.RAAaoULVMWYcFbjFLtwiCZUktF2pdjwDOv6zf0qiCl3t0130_provenance.
- NP702.RAAaoULVMWYcFbjFLtwiCZUktF2pdjwDOv6zf0qiCl3t0130_assertion evidence source_evidence_curated NP702.RAAaoULVMWYcFbjFLtwiCZUktF2pdjwDOv6zf0qiCl3t0130_provenance.
- NP702.RAAaoULVMWYcFbjFLtwiCZUktF2pdjwDOv6zf0qiCl3t0130_assertion SIO_000772 10732802 NP702.RAAaoULVMWYcFbjFLtwiCZUktF2pdjwDOv6zf0qiCl3t0130_provenance.
- NP702.RAAaoULVMWYcFbjFLtwiCZUktF2pdjwDOv6zf0qiCl3t0130_assertion wasDerivedFrom uniprot-2016 NP702.RAAaoULVMWYcFbjFLtwiCZUktF2pdjwDOv6zf0qiCl3t0130_provenance.
- NP702.RAAaoULVMWYcFbjFLtwiCZUktF2pdjwDOv6zf0qiCl3t0130_assertion wasGeneratedBy ECO_0000218 NP702.RAAaoULVMWYcFbjFLtwiCZUktF2pdjwDOv6zf0qiCl3t0130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP702.RAAaoULVMWYcFbjFLtwiCZUktF2pdjwDOv6zf0qiCl3t0130_provenance.