Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP153869.RA16kf77jhbbt1VPKp8nMkMjuTr1NM6MNlsjO5KG69n4c130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP153869.RA16kf77jhbbt1VPKp8nMkMjuTr1NM6MNlsjO5KG69n4c130_assertion type Assertion NP153869.RA16kf77jhbbt1VPKp8nMkMjuTr1NM6MNlsjO5KG69n4c130_head.
- NP153869.RA16kf77jhbbt1VPKp8nMkMjuTr1NM6MNlsjO5KG69n4c130_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." NP153869.RA16kf77jhbbt1VPKp8nMkMjuTr1NM6MNlsjO5KG69n4c130_provenance.
- NP153869.RA16kf77jhbbt1VPKp8nMkMjuTr1NM6MNlsjO5KG69n4c130_assertion evidence source_evidence_literature NP153869.RA16kf77jhbbt1VPKp8nMkMjuTr1NM6MNlsjO5KG69n4c130_provenance.
- NP153869.RA16kf77jhbbt1VPKp8nMkMjuTr1NM6MNlsjO5KG69n4c130_assertion SIO_000772 19651702 NP153869.RA16kf77jhbbt1VPKp8nMkMjuTr1NM6MNlsjO5KG69n4c130_provenance.
- NP153869.RA16kf77jhbbt1VPKp8nMkMjuTr1NM6MNlsjO5KG69n4c130_assertion wasDerivedFrom gad-20150221 NP153869.RA16kf77jhbbt1VPKp8nMkMjuTr1NM6MNlsjO5KG69n4c130_provenance.
- NP153869.RA16kf77jhbbt1VPKp8nMkMjuTr1NM6MNlsjO5KG69n4c130_assertion wasGeneratedBy ECO_0000203 NP153869.RA16kf77jhbbt1VPKp8nMkMjuTr1NM6MNlsjO5KG69n4c130_provenance.