Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_assertion> ?p ?o ?g. }
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- NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_assertion type Assertion NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_head.
- NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_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." NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_provenance.
- NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_assertion evidence source_evidence_literature NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_provenance.
- NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_assertion SIO_000772 11438993 NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_provenance.
- NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_assertion wasDerivedFrom befree-2016 NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_provenance.
- NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_assertion wasGeneratedBy ECO_0000203 NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_provenance.