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- source_evidence_literature type ECO_0000212 NP1223411.RAYZ36MS48RD8WZXK3g_izXv3sMSRr9NAqkCUqq0eKSdc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1223411.RAYZ36MS48RD8WZXK3g_izXv3sMSRr9NAqkCUqq0eKSdc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1223411.RAYZ36MS48RD8WZXK3g_izXv3sMSRr9NAqkCUqq0eKSdc130_provenance.
- NP1223411.RAYZ36MS48RD8WZXK3g_izXv3sMSRr9NAqkCUqq0eKSdc130_assertion description "[MTR was measured in the SN of patients with CMT type 1A (CMT1A, n = 10), CMT type 2A (CMT2A, n = 3), hereditary neuropathy with liability to pressure palsies (n = 3), and healthy controls (n = 21).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1223411.RAYZ36MS48RD8WZXK3g_izXv3sMSRr9NAqkCUqq0eKSdc130_provenance.
- NP1223411.RAYZ36MS48RD8WZXK3g_izXv3sMSRr9NAqkCUqq0eKSdc130_assertion evidence source_evidence_literature NP1223411.RAYZ36MS48RD8WZXK3g_izXv3sMSRr9NAqkCUqq0eKSdc130_provenance.
- NP1223411.RAYZ36MS48RD8WZXK3g_izXv3sMSRr9NAqkCUqq0eKSdc130_assertion SIO_000772 25253751 NP1223411.RAYZ36MS48RD8WZXK3g_izXv3sMSRr9NAqkCUqq0eKSdc130_provenance.
- NP1223411.RAYZ36MS48RD8WZXK3g_izXv3sMSRr9NAqkCUqq0eKSdc130_assertion wasDerivedFrom befree-2016 NP1223411.RAYZ36MS48RD8WZXK3g_izXv3sMSRr9NAqkCUqq0eKSdc130_provenance.
- NP1223411.RAYZ36MS48RD8WZXK3g_izXv3sMSRr9NAqkCUqq0eKSdc130_assertion wasGeneratedBy ECO_0000203 NP1223411.RAYZ36MS48RD8WZXK3g_izXv3sMSRr9NAqkCUqq0eKSdc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1223411.RAYZ36MS48RD8WZXK3g_izXv3sMSRr9NAqkCUqq0eKSdc130_provenance.