Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_provenance.
- NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_assertion description "[X-ALD is a neurological disorder associated with inherited defects in the ABCD1 (ALD) gene located on Xq28 and with impaired peroxisomal very long-chain fatty acid beta-oxidation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_provenance.
- NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_assertion evidence source_evidence_literature NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_provenance.
- NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_assertion SIO_000772 11438993 NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_provenance.
- NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_assertion wasDerivedFrom befree-20140225 NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_provenance.
- NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_assertion wasGeneratedBy ECO_0000203 NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_provenance.