Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP322903.RAMBSFTPL2fNsLktMcElaNf8NIhgLJZ6h3fhB_dJmf_lQ130_provenance.