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- source_evidence_literature type ECO_0000212 NP1395622.RAT3M1Yx5_uBFLK0dMRlz42BXdoLzHc_7YAlJf7w3FetU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1395622.RAT3M1Yx5_uBFLK0dMRlz42BXdoLzHc_7YAlJf7w3FetU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1395622.RAT3M1Yx5_uBFLK0dMRlz42BXdoLzHc_7YAlJf7w3FetU130_provenance.
- NP1395622.RAT3M1Yx5_uBFLK0dMRlz42BXdoLzHc_7YAlJf7w3FetU130_assertion description "[Linkage to 1p35-p36 (CMT2A), 3q (CMT2B), and 7p (CMT2D) chromosomes has been reported in the disease; however, most HMSN II families do not link to any of the reported loci.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1395622.RAT3M1Yx5_uBFLK0dMRlz42BXdoLzHc_7YAlJf7w3FetU130_provenance.
- NP1395622.RAT3M1Yx5_uBFLK0dMRlz42BXdoLzHc_7YAlJf7w3FetU130_assertion evidence source_evidence_literature NP1395622.RAT3M1Yx5_uBFLK0dMRlz42BXdoLzHc_7YAlJf7w3FetU130_provenance.
- NP1395622.RAT3M1Yx5_uBFLK0dMRlz42BXdoLzHc_7YAlJf7w3FetU130_assertion SIO_000772 9595994 NP1395622.RAT3M1Yx5_uBFLK0dMRlz42BXdoLzHc_7YAlJf7w3FetU130_provenance.
- NP1395622.RAT3M1Yx5_uBFLK0dMRlz42BXdoLzHc_7YAlJf7w3FetU130_assertion wasDerivedFrom befree-2016 NP1395622.RAT3M1Yx5_uBFLK0dMRlz42BXdoLzHc_7YAlJf7w3FetU130_provenance.
- NP1395622.RAT3M1Yx5_uBFLK0dMRlz42BXdoLzHc_7YAlJf7w3FetU130_assertion wasGeneratedBy ECO_0000203 NP1395622.RAT3M1Yx5_uBFLK0dMRlz42BXdoLzHc_7YAlJf7w3FetU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1395622.RAT3M1Yx5_uBFLK0dMRlz42BXdoLzHc_7YAlJf7w3FetU130_provenance.