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- source_evidence_literature type ECO_0000212 NP418999.RA-fiRlqj5FgHrgw5PVEX5utjDH06B__YBwp7-1j94Pgc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418999.RA-fiRlqj5FgHrgw5PVEX5utjDH06B__YBwp7-1j94Pgc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418999.RA-fiRlqj5FgHrgw5PVEX5utjDH06B__YBwp7-1j94Pgc130_provenance.
- NP418999.RA-fiRlqj5FgHrgw5PVEX5utjDH06B__YBwp7-1j94Pgc130_assertion description "[In analogy to symptomatic female dystrophinopathy carriers, our results suggest that heterozygous alpha-sarcoglycan gene mutation carriers can be symptomatic with selective muscle weakness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418999.RA-fiRlqj5FgHrgw5PVEX5utjDH06B__YBwp7-1j94Pgc130_provenance.
- NP418999.RA-fiRlqj5FgHrgw5PVEX5utjDH06B__YBwp7-1j94Pgc130_assertion evidence source_evidence_literature NP418999.RA-fiRlqj5FgHrgw5PVEX5utjDH06B__YBwp7-1j94Pgc130_provenance.
- NP418999.RA-fiRlqj5FgHrgw5PVEX5utjDH06B__YBwp7-1j94Pgc130_assertion SIO_000772 14595658 NP418999.RA-fiRlqj5FgHrgw5PVEX5utjDH06B__YBwp7-1j94Pgc130_provenance.
- NP418999.RA-fiRlqj5FgHrgw5PVEX5utjDH06B__YBwp7-1j94Pgc130_assertion wasDerivedFrom befree-2016 NP418999.RA-fiRlqj5FgHrgw5PVEX5utjDH06B__YBwp7-1j94Pgc130_provenance.
- NP418999.RA-fiRlqj5FgHrgw5PVEX5utjDH06B__YBwp7-1j94Pgc130_assertion wasGeneratedBy ECO_0000203 NP418999.RA-fiRlqj5FgHrgw5PVEX5utjDH06B__YBwp7-1j94Pgc130_provenance.
- befree-2016 importedOn "2016-02-19" NP418999.RA-fiRlqj5FgHrgw5PVEX5utjDH06B__YBwp7-1j94Pgc130_provenance.