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- source_evidence_literature type ECO_0000212 NP298248.RAs4f-t7hfWzDUL4bDDd0HO-xeu14IpZL8r4PpZ3zJF8E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP298248.RAs4f-t7hfWzDUL4bDDd0HO-xeu14IpZL8r4PpZ3zJF8E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP298248.RAs4f-t7hfWzDUL4bDDd0HO-xeu14IpZL8r4PpZ3zJF8E130_provenance.
- NP298248.RAs4f-t7hfWzDUL4bDDd0HO-xeu14IpZL8r4PpZ3zJF8E130_assertion description "[So far, disease-associated mutations have been identified in seven genes: two genes for autosomal dominant (SPTLC1 and RAB7) and five genes for autosomal recessive forms of HSAN (WNK1/HSN2, NTRK1, NGFB, CCT5 and IKBKAP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP298248.RAs4f-t7hfWzDUL4bDDd0HO-xeu14IpZL8r4PpZ3zJF8E130_provenance.
- NP298248.RAs4f-t7hfWzDUL4bDDd0HO-xeu14IpZL8r4PpZ3zJF8E130_assertion evidence source_evidence_literature NP298248.RAs4f-t7hfWzDUL4bDDd0HO-xeu14IpZL8r4PpZ3zJF8E130_provenance.
- NP298248.RAs4f-t7hfWzDUL4bDDd0HO-xeu14IpZL8r4PpZ3zJF8E130_assertion SIO_000772 19651702 NP298248.RAs4f-t7hfWzDUL4bDDd0HO-xeu14IpZL8r4PpZ3zJF8E130_provenance.
- NP298248.RAs4f-t7hfWzDUL4bDDd0HO-xeu14IpZL8r4PpZ3zJF8E130_assertion wasDerivedFrom befree-20140225 NP298248.RAs4f-t7hfWzDUL4bDDd0HO-xeu14IpZL8r4PpZ3zJF8E130_provenance.
- NP298248.RAs4f-t7hfWzDUL4bDDd0HO-xeu14IpZL8r4PpZ3zJF8E130_assertion wasGeneratedBy ECO_0000203 NP298248.RAs4f-t7hfWzDUL4bDDd0HO-xeu14IpZL8r4PpZ3zJF8E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP298248.RAs4f-t7hfWzDUL4bDDd0HO-xeu14IpZL8r4PpZ3zJF8E130_provenance.