Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP722644.RAbi3mvG1IW_EA5k8zPbvRsWbODHBWWb16vE-mL6H-AIA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP722644.RAbi3mvG1IW_EA5k8zPbvRsWbODHBWWb16vE-mL6H-AIA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP722644.RAbi3mvG1IW_EA5k8zPbvRsWbODHBWWb16vE-mL6H-AIA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP722644.RAbi3mvG1IW_EA5k8zPbvRsWbODHBWWb16vE-mL6H-AIA130_provenance.
- NP722644.RAbi3mvG1IW_EA5k8zPbvRsWbODHBWWb16vE-mL6H-AIA130_assertion description "[We report the molecular findings in 14 patients (12 families) with X-linked adrenoleukodystrophy (X-ALD, MIM# 300100), a well-defined peroxisomal disorder attributed to mutations in the ABCD1 gene on chromosome Xq28.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP722644.RAbi3mvG1IW_EA5k8zPbvRsWbODHBWWb16vE-mL6H-AIA130_provenance.
- NP722644.RAbi3mvG1IW_EA5k8zPbvRsWbODHBWWb16vE-mL6H-AIA130_assertion evidence source_evidence_literature NP722644.RAbi3mvG1IW_EA5k8zPbvRsWbODHBWWb16vE-mL6H-AIA130_provenance.
- NP722644.RAbi3mvG1IW_EA5k8zPbvRsWbODHBWWb16vE-mL6H-AIA130_assertion SIO_000772 15643618 NP722644.RAbi3mvG1IW_EA5k8zPbvRsWbODHBWWb16vE-mL6H-AIA130_provenance.
- NP722644.RAbi3mvG1IW_EA5k8zPbvRsWbODHBWWb16vE-mL6H-AIA130_assertion wasDerivedFrom befree-20140225 NP722644.RAbi3mvG1IW_EA5k8zPbvRsWbODHBWWb16vE-mL6H-AIA130_provenance.
- NP722644.RAbi3mvG1IW_EA5k8zPbvRsWbODHBWWb16vE-mL6H-AIA130_assertion wasGeneratedBy ECO_0000203 NP722644.RAbi3mvG1IW_EA5k8zPbvRsWbODHBWWb16vE-mL6H-AIA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP722644.RAbi3mvG1IW_EA5k8zPbvRsWbODHBWWb16vE-mL6H-AIA130_provenance.