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- source_evidence_literature type ECO_0000212 NP475811.RAZcfNurrf45qtsbcmOTBkiyaDkpG4OTd6AnAkzXv1lJA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP475811.RAZcfNurrf45qtsbcmOTBkiyaDkpG4OTd6AnAkzXv1lJA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP475811.RAZcfNurrf45qtsbcmOTBkiyaDkpG4OTd6AnAkzXv1lJA130_provenance.
- NP475811.RAZcfNurrf45qtsbcmOTBkiyaDkpG4OTd6AnAkzXv1lJA130_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." NP475811.RAZcfNurrf45qtsbcmOTBkiyaDkpG4OTd6AnAkzXv1lJA130_provenance.
- NP475811.RAZcfNurrf45qtsbcmOTBkiyaDkpG4OTd6AnAkzXv1lJA130_assertion evidence source_evidence_literature NP475811.RAZcfNurrf45qtsbcmOTBkiyaDkpG4OTd6AnAkzXv1lJA130_provenance.
- NP475811.RAZcfNurrf45qtsbcmOTBkiyaDkpG4OTd6AnAkzXv1lJA130_assertion SIO_000772 15643618 NP475811.RAZcfNurrf45qtsbcmOTBkiyaDkpG4OTd6AnAkzXv1lJA130_provenance.
- NP475811.RAZcfNurrf45qtsbcmOTBkiyaDkpG4OTd6AnAkzXv1lJA130_assertion wasDerivedFrom befree-2016 NP475811.RAZcfNurrf45qtsbcmOTBkiyaDkpG4OTd6AnAkzXv1lJA130_provenance.
- NP475811.RAZcfNurrf45qtsbcmOTBkiyaDkpG4OTd6AnAkzXv1lJA130_assertion wasGeneratedBy ECO_0000203 NP475811.RAZcfNurrf45qtsbcmOTBkiyaDkpG4OTd6AnAkzXv1lJA130_provenance.
- befree-2016 importedOn "2016-02-19" NP475811.RAZcfNurrf45qtsbcmOTBkiyaDkpG4OTd6AnAkzXv1lJA130_provenance.