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- source_evidence_literature type ECO_0000212 NP1186887.RA-yg612_PCPSA131QDlYXei7uXfGicDVwVvdKL_EtB4c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1186887.RA-yg612_PCPSA131QDlYXei7uXfGicDVwVvdKL_EtB4c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1186887.RA-yg612_PCPSA131QDlYXei7uXfGicDVwVvdKL_EtB4c130_provenance.
- NP1186887.RA-yg612_PCPSA131QDlYXei7uXfGicDVwVvdKL_EtB4c130_assertion description "[Disorders with a known molecular basis falling within this group include hereditary neuropathy with liability to pressure palsies (HNPP) due to the deletion of the PMP22 gene or to mutations in this same gene, and hereditary neuralgic amyotrophy (HNA) caused by mutations in the SEPT9 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1186887.RA-yg612_PCPSA131QDlYXei7uXfGicDVwVvdKL_EtB4c130_provenance.
- NP1186887.RA-yg612_PCPSA131QDlYXei7uXfGicDVwVvdKL_EtB4c130_assertion evidence source_evidence_literature NP1186887.RA-yg612_PCPSA131QDlYXei7uXfGicDVwVvdKL_EtB4c130_provenance.
- NP1186887.RA-yg612_PCPSA131QDlYXei7uXfGicDVwVvdKL_EtB4c130_assertion SIO_000772 24878226 NP1186887.RA-yg612_PCPSA131QDlYXei7uXfGicDVwVvdKL_EtB4c130_provenance.
- NP1186887.RA-yg612_PCPSA131QDlYXei7uXfGicDVwVvdKL_EtB4c130_assertion wasDerivedFrom befree-2016 NP1186887.RA-yg612_PCPSA131QDlYXei7uXfGicDVwVvdKL_EtB4c130_provenance.
- NP1186887.RA-yg612_PCPSA131QDlYXei7uXfGicDVwVvdKL_EtB4c130_assertion wasGeneratedBy ECO_0000203 NP1186887.RA-yg612_PCPSA131QDlYXei7uXfGicDVwVvdKL_EtB4c130_provenance.
- befree-2016 importedOn "2016-02-19" NP1186887.RA-yg612_PCPSA131QDlYXei7uXfGicDVwVvdKL_EtB4c130_provenance.