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- source_evidence_literature type ECO_0000212 NP661579.RALr49z73VOWKZL6TF_HWsy6NdSyIcVUzyhKfL5OGL594130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP661579.RALr49z73VOWKZL6TF_HWsy6NdSyIcVUzyhKfL5OGL594130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP661579.RALr49z73VOWKZL6TF_HWsy6NdSyIcVUzyhKfL5OGL594130_provenance.
- NP661579.RALr49z73VOWKZL6TF_HWsy6NdSyIcVUzyhKfL5OGL594130_assertion description "[With the aim of developing an algorithm for the etiological diagnosis of primary adrenal insufficiency, we studied 56 Italian patients with nonsurgical primary adrenal insufficiency and 24 French patients with X-linked adrenoleukodystrophy (ALD) for serum levels of adrenal cortex, steroid-21-hydroxylase (21OHAb), islet cell (ICA), glutamate decarboxylase (GAD65Ab), IA2/ICA512 (ICA512Ab), thyroid peroxidase (TPOAb) autoantibodies, and plasmatic concentrations of very long chain fatty acids (VLCFA).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661579.RALr49z73VOWKZL6TF_HWsy6NdSyIcVUzyhKfL5OGL594130_provenance.
- NP661579.RALr49z73VOWKZL6TF_HWsy6NdSyIcVUzyhKfL5OGL594130_assertion evidence source_evidence_literature NP661579.RALr49z73VOWKZL6TF_HWsy6NdSyIcVUzyhKfL5OGL594130_provenance.
- NP661579.RALr49z73VOWKZL6TF_HWsy6NdSyIcVUzyhKfL5OGL594130_assertion SIO_000772 9745420 NP661579.RALr49z73VOWKZL6TF_HWsy6NdSyIcVUzyhKfL5OGL594130_provenance.
- NP661579.RALr49z73VOWKZL6TF_HWsy6NdSyIcVUzyhKfL5OGL594130_assertion wasDerivedFrom befree-20150227 NP661579.RALr49z73VOWKZL6TF_HWsy6NdSyIcVUzyhKfL5OGL594130_provenance.
- NP661579.RALr49z73VOWKZL6TF_HWsy6NdSyIcVUzyhKfL5OGL594130_assertion wasGeneratedBy ECO_0000203 NP661579.RALr49z73VOWKZL6TF_HWsy6NdSyIcVUzyhKfL5OGL594130_provenance.
- befree-20150227 importedOn "2015-02-27" NP661579.RALr49z73VOWKZL6TF_HWsy6NdSyIcVUzyhKfL5OGL594130_provenance.