Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP72756.RAhMPLjTNPlv-0iD5lz-DzNtGkET00kpF8bpyTjf44JkE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP72756.RAhMPLjTNPlv-0iD5lz-DzNtGkET00kpF8bpyTjf44JkE130_assertion type Assertion NP72756.RAhMPLjTNPlv-0iD5lz-DzNtGkET00kpF8bpyTjf44JkE130_head.
- NP72756.RAhMPLjTNPlv-0iD5lz-DzNtGkET00kpF8bpyTjf44JkE130_assertion wasGeneratedBy ECO_0000203 NP72756.RAhMPLjTNPlv-0iD5lz-DzNtGkET00kpF8bpyTjf44JkE130_provenance.
- NP72756.RAhMPLjTNPlv-0iD5lz-DzNtGkET00kpF8bpyTjf44JkE130_assertion wasDerivedFrom gad-20130706 NP72756.RAhMPLjTNPlv-0iD5lz-DzNtGkET00kpF8bpyTjf44JkE130_provenance.
- NP72756.RAhMPLjTNPlv-0iD5lz-DzNtGkET00kpF8bpyTjf44JkE130_assertion SIO_000772 19651702 NP72756.RAhMPLjTNPlv-0iD5lz-DzNtGkET00kpF8bpyTjf44JkE130_provenance.
- NP72756.RAhMPLjTNPlv-0iD5lz-DzNtGkET00kpF8bpyTjf44JkE130_assertion evidence source_evidence_literature NP72756.RAhMPLjTNPlv-0iD5lz-DzNtGkET00kpF8bpyTjf44JkE130_provenance.
- NP72756.RAhMPLjTNPlv-0iD5lz-DzNtGkET00kpF8bpyTjf44JkE130_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." NP72756.RAhMPLjTNPlv-0iD5lz-DzNtGkET00kpF8bpyTjf44JkE130_provenance.