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- NP89718.RAloCELpNScN4Wj_6VWU0IkMxVFJasQHZqHvBGk58XdcY130_assertion type Assertion NP89718.RAloCELpNScN4Wj_6VWU0IkMxVFJasQHZqHvBGk58XdcY130_head.
- NP89718.RAloCELpNScN4Wj_6VWU0IkMxVFJasQHZqHvBGk58XdcY130_assertion wasGeneratedBy ECO_0000203 NP89718.RAloCELpNScN4Wj_6VWU0IkMxVFJasQHZqHvBGk58XdcY130_provenance.
- NP89718.RAloCELpNScN4Wj_6VWU0IkMxVFJasQHZqHvBGk58XdcY130_assertion wasDerivedFrom gad-20150221 NP89718.RAloCELpNScN4Wj_6VWU0IkMxVFJasQHZqHvBGk58XdcY130_provenance.
- NP89718.RAloCELpNScN4Wj_6VWU0IkMxVFJasQHZqHvBGk58XdcY130_assertion SIO_000772 19651702 NP89718.RAloCELpNScN4Wj_6VWU0IkMxVFJasQHZqHvBGk58XdcY130_provenance.
- NP89718.RAloCELpNScN4Wj_6VWU0IkMxVFJasQHZqHvBGk58XdcY130_assertion evidence source_evidence_literature NP89718.RAloCELpNScN4Wj_6VWU0IkMxVFJasQHZqHvBGk58XdcY130_provenance.
- NP89718.RAloCELpNScN4Wj_6VWU0IkMxVFJasQHZqHvBGk58XdcY130_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." NP89718.RAloCELpNScN4Wj_6VWU0IkMxVFJasQHZqHvBGk58XdcY130_provenance.