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- source_evidence_literature type ECO_0000212 NP568254.RAThfcQlqio_TqLK51LDTB72pBEEJmXREqM0gOkaR-42Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP568254.RAThfcQlqio_TqLK51LDTB72pBEEJmXREqM0gOkaR-42Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP568254.RAThfcQlqio_TqLK51LDTB72pBEEJmXREqM0gOkaR-42Q130_provenance.
- NP568254.RAThfcQlqio_TqLK51LDTB72pBEEJmXREqM0gOkaR-42Q130_assertion description "[The Val102fs mutation of the myelin protein zero gene (MPZ) has been associated with Charcot-Marie-Tooth disease type 1B (CMT1B).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP568254.RAThfcQlqio_TqLK51LDTB72pBEEJmXREqM0gOkaR-42Q130_provenance.
- NP568254.RAThfcQlqio_TqLK51LDTB72pBEEJmXREqM0gOkaR-42Q130_assertion evidence source_evidence_literature NP568254.RAThfcQlqio_TqLK51LDTB72pBEEJmXREqM0gOkaR-42Q130_provenance.
- NP568254.RAThfcQlqio_TqLK51LDTB72pBEEJmXREqM0gOkaR-42Q130_assertion SIO_000772 19906531 NP568254.RAThfcQlqio_TqLK51LDTB72pBEEJmXREqM0gOkaR-42Q130_provenance.
- NP568254.RAThfcQlqio_TqLK51LDTB72pBEEJmXREqM0gOkaR-42Q130_assertion wasDerivedFrom befree-20150227 NP568254.RAThfcQlqio_TqLK51LDTB72pBEEJmXREqM0gOkaR-42Q130_provenance.
- NP568254.RAThfcQlqio_TqLK51LDTB72pBEEJmXREqM0gOkaR-42Q130_assertion wasGeneratedBy ECO_0000203 NP568254.RAThfcQlqio_TqLK51LDTB72pBEEJmXREqM0gOkaR-42Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP568254.RAThfcQlqio_TqLK51LDTB72pBEEJmXREqM0gOkaR-42Q130_provenance.