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- source_evidence_literature type ECO_0000212 NP234076.RAhCamYoNmv3l6GJG5otFMKcnj54oqb2U38dKY74LZi78130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP234076.RAhCamYoNmv3l6GJG5otFMKcnj54oqb2U38dKY74LZi78130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP234076.RAhCamYoNmv3l6GJG5otFMKcnj54oqb2U38dKY74LZi78130_provenance.
- NP234076.RAhCamYoNmv3l6GJG5otFMKcnj54oqb2U38dKY74LZi78130_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." NP234076.RAhCamYoNmv3l6GJG5otFMKcnj54oqb2U38dKY74LZi78130_provenance.
- NP234076.RAhCamYoNmv3l6GJG5otFMKcnj54oqb2U38dKY74LZi78130_assertion evidence source_evidence_literature NP234076.RAhCamYoNmv3l6GJG5otFMKcnj54oqb2U38dKY74LZi78130_provenance.
- NP234076.RAhCamYoNmv3l6GJG5otFMKcnj54oqb2U38dKY74LZi78130_assertion SIO_000772 15643618 NP234076.RAhCamYoNmv3l6GJG5otFMKcnj54oqb2U38dKY74LZi78130_provenance.
- NP234076.RAhCamYoNmv3l6GJG5otFMKcnj54oqb2U38dKY74LZi78130_assertion wasDerivedFrom befree-20150227 NP234076.RAhCamYoNmv3l6GJG5otFMKcnj54oqb2U38dKY74LZi78130_provenance.
- NP234076.RAhCamYoNmv3l6GJG5otFMKcnj54oqb2U38dKY74LZi78130_assertion wasGeneratedBy ECO_0000203 NP234076.RAhCamYoNmv3l6GJG5otFMKcnj54oqb2U38dKY74LZi78130_provenance.
- befree-20150227 importedOn "2015-02-27" NP234076.RAhCamYoNmv3l6GJG5otFMKcnj54oqb2U38dKY74LZi78130_provenance.