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- source_evidence_literature type ECO_0000212 NP1362969.RA4aGpINFq3t-a6q08zJguJGuFjxXiBO1QIFZJTFvTyVE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1362969.RA4aGpINFq3t-a6q08zJguJGuFjxXiBO1QIFZJTFvTyVE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1362969.RA4aGpINFq3t-a6q08zJguJGuFjxXiBO1QIFZJTFvTyVE130_provenance.
- NP1362969.RA4aGpINFq3t-a6q08zJguJGuFjxXiBO1QIFZJTFvTyVE130_assertion description "[We used the fluorescence-assisted mismatch analysis (FAMA) method to screen rapidly the alpha-galactosidase A gene in patients with Fabry disease in order to identify unknown mutations and help define genotype-phenotype correlations in this X-linked lysosomal storage disorder.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1362969.RA4aGpINFq3t-a6q08zJguJGuFjxXiBO1QIFZJTFvTyVE130_provenance.
- NP1362969.RA4aGpINFq3t-a6q08zJguJGuFjxXiBO1QIFZJTFvTyVE130_assertion evidence source_evidence_literature NP1362969.RA4aGpINFq3t-a6q08zJguJGuFjxXiBO1QIFZJTFvTyVE130_provenance.
- NP1362969.RA4aGpINFq3t-a6q08zJguJGuFjxXiBO1QIFZJTFvTyVE130_assertion SIO_000772 8931708 NP1362969.RA4aGpINFq3t-a6q08zJguJGuFjxXiBO1QIFZJTFvTyVE130_provenance.
- NP1362969.RA4aGpINFq3t-a6q08zJguJGuFjxXiBO1QIFZJTFvTyVE130_assertion wasDerivedFrom befree-2016 NP1362969.RA4aGpINFq3t-a6q08zJguJGuFjxXiBO1QIFZJTFvTyVE130_provenance.
- NP1362969.RA4aGpINFq3t-a6q08zJguJGuFjxXiBO1QIFZJTFvTyVE130_assertion wasGeneratedBy ECO_0000203 NP1362969.RA4aGpINFq3t-a6q08zJguJGuFjxXiBO1QIFZJTFvTyVE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1362969.RA4aGpINFq3t-a6q08zJguJGuFjxXiBO1QIFZJTFvTyVE130_provenance.