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- source_evidence_literature type ECO_0000212 NP76798.RA_NeBN-oKKz5SNzKCFjmPCigDpY2hnQhC_Sy9C-zIqJA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP76798.RA_NeBN-oKKz5SNzKCFjmPCigDpY2hnQhC_Sy9C-zIqJA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP76798.RA_NeBN-oKKz5SNzKCFjmPCigDpY2hnQhC_Sy9C-zIqJA130_provenance.
- NP76798.RA_NeBN-oKKz5SNzKCFjmPCigDpY2hnQhC_Sy9C-zIqJA130_assertion description "[Our results indicate that LGMD2A is one of the most frequent autosomal recessive disorders, thus finding its molecular characterization becoming increasingly important.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP76798.RA_NeBN-oKKz5SNzKCFjmPCigDpY2hnQhC_Sy9C-zIqJA130_provenance.
- NP76798.RA_NeBN-oKKz5SNzKCFjmPCigDpY2hnQhC_Sy9C-zIqJA130_assertion evidence source_evidence_literature NP76798.RA_NeBN-oKKz5SNzKCFjmPCigDpY2hnQhC_Sy9C-zIqJA130_provenance.
- NP76798.RA_NeBN-oKKz5SNzKCFjmPCigDpY2hnQhC_Sy9C-zIqJA130_assertion SIO_000772 15725583 NP76798.RA_NeBN-oKKz5SNzKCFjmPCigDpY2hnQhC_Sy9C-zIqJA130_provenance.
- NP76798.RA_NeBN-oKKz5SNzKCFjmPCigDpY2hnQhC_Sy9C-zIqJA130_assertion wasDerivedFrom gad-20150221 NP76798.RA_NeBN-oKKz5SNzKCFjmPCigDpY2hnQhC_Sy9C-zIqJA130_provenance.
- NP76798.RA_NeBN-oKKz5SNzKCFjmPCigDpY2hnQhC_Sy9C-zIqJA130_assertion wasGeneratedBy ECO_0000203 NP76798.RA_NeBN-oKKz5SNzKCFjmPCigDpY2hnQhC_Sy9C-zIqJA130_provenance.
- gad-20150221 importedOn "2015-02-21" NP76798.RA_NeBN-oKKz5SNzKCFjmPCigDpY2hnQhC_Sy9C-zIqJA130_provenance.