Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP924998.RAfb7OqhHbSOe4GqATe94p2hmCQ9wjw2MK1wKr76Z8SBI130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP924998.RAfb7OqhHbSOe4GqATe94p2hmCQ9wjw2MK1wKr76Z8SBI130_assertion type Assertion NP924998.RAfb7OqhHbSOe4GqATe94p2hmCQ9wjw2MK1wKr76Z8SBI130_head.
- NP924998.RAfb7OqhHbSOe4GqATe94p2hmCQ9wjw2MK1wKr76Z8SBI130_assertion description "[This patient broadens the spectrum of SLC9A6 mutations and contributes to the clinical delineation of Christianson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924998.RAfb7OqhHbSOe4GqATe94p2hmCQ9wjw2MK1wKr76Z8SBI130_provenance.
- NP924998.RAfb7OqhHbSOe4GqATe94p2hmCQ9wjw2MK1wKr76Z8SBI130_assertion evidence source_evidence_literature NP924998.RAfb7OqhHbSOe4GqATe94p2hmCQ9wjw2MK1wKr76Z8SBI130_provenance.
- NP924998.RAfb7OqhHbSOe4GqATe94p2hmCQ9wjw2MK1wKr76Z8SBI130_assertion SIO_000772 21932316 NP924998.RAfb7OqhHbSOe4GqATe94p2hmCQ9wjw2MK1wKr76Z8SBI130_provenance.
- NP924998.RAfb7OqhHbSOe4GqATe94p2hmCQ9wjw2MK1wKr76Z8SBI130_assertion wasDerivedFrom befree-2016 NP924998.RAfb7OqhHbSOe4GqATe94p2hmCQ9wjw2MK1wKr76Z8SBI130_provenance.
- NP924998.RAfb7OqhHbSOe4GqATe94p2hmCQ9wjw2MK1wKr76Z8SBI130_assertion wasGeneratedBy ECO_0000203 NP924998.RAfb7OqhHbSOe4GqATe94p2hmCQ9wjw2MK1wKr76Z8SBI130_provenance.