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- source_evidence_literature type ECO_0000212 NP883166.RAJl582DIp8tcbX7iynd05KgKRoR4iUH3-H6OGo5jHmlM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP883166.RAJl582DIp8tcbX7iynd05KgKRoR4iUH3-H6OGo5jHmlM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP883166.RAJl582DIp8tcbX7iynd05KgKRoR4iUH3-H6OGo5jHmlM130_provenance.
- NP883166.RAJl582DIp8tcbX7iynd05KgKRoR4iUH3-H6OGo5jHmlM130_assertion description "[The Pro56Ser mutation in the human VAPB MSP domain causes a familial amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP883166.RAJl582DIp8tcbX7iynd05KgKRoR4iUH3-H6OGo5jHmlM130_provenance.
- NP883166.RAJl582DIp8tcbX7iynd05KgKRoR4iUH3-H6OGo5jHmlM130_assertion evidence source_evidence_literature NP883166.RAJl582DIp8tcbX7iynd05KgKRoR4iUH3-H6OGo5jHmlM130_provenance.
- NP883166.RAJl582DIp8tcbX7iynd05KgKRoR4iUH3-H6OGo5jHmlM130_assertion SIO_000772 20377183 NP883166.RAJl582DIp8tcbX7iynd05KgKRoR4iUH3-H6OGo5jHmlM130_provenance.
- NP883166.RAJl582DIp8tcbX7iynd05KgKRoR4iUH3-H6OGo5jHmlM130_assertion wasDerivedFrom befree-20140225 NP883166.RAJl582DIp8tcbX7iynd05KgKRoR4iUH3-H6OGo5jHmlM130_provenance.
- NP883166.RAJl582DIp8tcbX7iynd05KgKRoR4iUH3-H6OGo5jHmlM130_assertion wasGeneratedBy ECO_0000203 NP883166.RAJl582DIp8tcbX7iynd05KgKRoR4iUH3-H6OGo5jHmlM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP883166.RAJl582DIp8tcbX7iynd05KgKRoR4iUH3-H6OGo5jHmlM130_provenance.