Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_assertion> ?p ?o ?g. }
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- NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_assertion type Assertion NP332601.RAcjA6me7AMx_ovmhQW8Cc_uJGPjWWGdjVgxhXONh-FBE130_head.
- 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.