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- source_evidence_literature type ECO_0000212 NP733331.RANm68zkEsgnNiDQiuM-YaFANpHi2YU9kvvU_GKN5PPrU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP733331.RANm68zkEsgnNiDQiuM-YaFANpHi2YU9kvvU_GKN5PPrU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP733331.RANm68zkEsgnNiDQiuM-YaFANpHi2YU9kvvU_GKN5PPrU130_provenance.
- NP733331.RANm68zkEsgnNiDQiuM-YaFANpHi2YU9kvvU_GKN5PPrU130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP733331.RANm68zkEsgnNiDQiuM-YaFANpHi2YU9kvvU_GKN5PPrU130_provenance.
- NP733331.RANm68zkEsgnNiDQiuM-YaFANpHi2YU9kvvU_GKN5PPrU130_assertion evidence source_evidence_literature NP733331.RANm68zkEsgnNiDQiuM-YaFANpHi2YU9kvvU_GKN5PPrU130_provenance.
- NP733331.RANm68zkEsgnNiDQiuM-YaFANpHi2YU9kvvU_GKN5PPrU130_assertion SIO_000772 19378506 NP733331.RANm68zkEsgnNiDQiuM-YaFANpHi2YU9kvvU_GKN5PPrU130_provenance.
- NP733331.RANm68zkEsgnNiDQiuM-YaFANpHi2YU9kvvU_GKN5PPrU130_assertion wasDerivedFrom befree-2016 NP733331.RANm68zkEsgnNiDQiuM-YaFANpHi2YU9kvvU_GKN5PPrU130_provenance.
- NP733331.RANm68zkEsgnNiDQiuM-YaFANpHi2YU9kvvU_GKN5PPrU130_assertion wasGeneratedBy ECO_0000203 NP733331.RANm68zkEsgnNiDQiuM-YaFANpHi2YU9kvvU_GKN5PPrU130_provenance.
- befree-2016 importedOn "2016-02-19" NP733331.RANm68zkEsgnNiDQiuM-YaFANpHi2YU9kvvU_GKN5PPrU130_provenance.