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- source_evidence_literature type ECO_0000212 NP1081847.RAMrc0BFa1l7Kz-Hs_vY8XACUDe8vAkGfg1nngaZhukSc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1081847.RAMrc0BFa1l7Kz-Hs_vY8XACUDe8vAkGfg1nngaZhukSc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1081847.RAMrc0BFa1l7Kz-Hs_vY8XACUDe8vAkGfg1nngaZhukSc130_provenance.
- NP1081847.RAMrc0BFa1l7Kz-Hs_vY8XACUDe8vAkGfg1nngaZhukSc130_assertion description "[Huntington's disease (HD) is a neurodegenerative disorder caused by an abnormal expansion of a CAG repeat encoding a polyglutamine tract in the huntingtin (Htt) protein.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1081847.RAMrc0BFa1l7Kz-Hs_vY8XACUDe8vAkGfg1nngaZhukSc130_provenance.
- NP1081847.RAMrc0BFa1l7Kz-Hs_vY8XACUDe8vAkGfg1nngaZhukSc130_assertion evidence source_evidence_literature NP1081847.RAMrc0BFa1l7Kz-Hs_vY8XACUDe8vAkGfg1nngaZhukSc130_provenance.
- NP1081847.RAMrc0BFa1l7Kz-Hs_vY8XACUDe8vAkGfg1nngaZhukSc130_assertion SIO_000772 23720495 NP1081847.RAMrc0BFa1l7Kz-Hs_vY8XACUDe8vAkGfg1nngaZhukSc130_provenance.
- NP1081847.RAMrc0BFa1l7Kz-Hs_vY8XACUDe8vAkGfg1nngaZhukSc130_assertion wasDerivedFrom befree-2016 NP1081847.RAMrc0BFa1l7Kz-Hs_vY8XACUDe8vAkGfg1nngaZhukSc130_provenance.
- NP1081847.RAMrc0BFa1l7Kz-Hs_vY8XACUDe8vAkGfg1nngaZhukSc130_assertion wasGeneratedBy ECO_0000203 NP1081847.RAMrc0BFa1l7Kz-Hs_vY8XACUDe8vAkGfg1nngaZhukSc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1081847.RAMrc0BFa1l7Kz-Hs_vY8XACUDe8vAkGfg1nngaZhukSc130_provenance.