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- source_evidence_literature type ECO_0000212 NP322900.RA8J_JDAACq5ylI6uDcsgNab1IAO3BIPpy3vT8Gw5NQnE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP322900.RA8J_JDAACq5ylI6uDcsgNab1IAO3BIPpy3vT8Gw5NQnE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP322900.RA8J_JDAACq5ylI6uDcsgNab1IAO3BIPpy3vT8Gw5NQnE130_provenance.
- NP322900.RA8J_JDAACq5ylI6uDcsgNab1IAO3BIPpy3vT8Gw5NQnE130_assertion description "[Charcot-Marie-Tooth neuropathy type 1 (CMT1), the most common hereditary neurological disorder in humans, is characterized by clinical and genetic heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP322900.RA8J_JDAACq5ylI6uDcsgNab1IAO3BIPpy3vT8Gw5NQnE130_provenance.
- NP322900.RA8J_JDAACq5ylI6uDcsgNab1IAO3BIPpy3vT8Gw5NQnE130_assertion evidence source_evidence_literature NP322900.RA8J_JDAACq5ylI6uDcsgNab1IAO3BIPpy3vT8Gw5NQnE130_provenance.
- NP322900.RA8J_JDAACq5ylI6uDcsgNab1IAO3BIPpy3vT8Gw5NQnE130_assertion SIO_000772 11438991 NP322900.RA8J_JDAACq5ylI6uDcsgNab1IAO3BIPpy3vT8Gw5NQnE130_provenance.
- NP322900.RA8J_JDAACq5ylI6uDcsgNab1IAO3BIPpy3vT8Gw5NQnE130_assertion wasDerivedFrom befree-2016 NP322900.RA8J_JDAACq5ylI6uDcsgNab1IAO3BIPpy3vT8Gw5NQnE130_provenance.
- NP322900.RA8J_JDAACq5ylI6uDcsgNab1IAO3BIPpy3vT8Gw5NQnE130_assertion wasGeneratedBy ECO_0000203 NP322900.RA8J_JDAACq5ylI6uDcsgNab1IAO3BIPpy3vT8Gw5NQnE130_provenance.
- befree-2016 importedOn "2016-02-19" NP322900.RA8J_JDAACq5ylI6uDcsgNab1IAO3BIPpy3vT8Gw5NQnE130_provenance.