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- NP508.RA06ck0MWmeMR9GodMpYsCVAlwORnoBhq1n9ie9bJvfTI130_assertion type Assertion NP508.RA06ck0MWmeMR9GodMpYsCVAlwORnoBhq1n9ie9bJvfTI130_head.
- NP508.RA06ck0MWmeMR9GodMpYsCVAlwORnoBhq1n9ie9bJvfTI130_assertion description "[We found a homozygous SLC17A5 mutation (R39C) in five Finnish patients with Salla disease and six different SLC17A5 mutations in six ISSD patients of different ethnic origins.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP508.RA06ck0MWmeMR9GodMpYsCVAlwORnoBhq1n9ie9bJvfTI130_provenance.
- NP508.RA06ck0MWmeMR9GodMpYsCVAlwORnoBhq1n9ie9bJvfTI130_assertion evidence source_evidence_curated NP508.RA06ck0MWmeMR9GodMpYsCVAlwORnoBhq1n9ie9bJvfTI130_provenance.
- NP508.RA06ck0MWmeMR9GodMpYsCVAlwORnoBhq1n9ie9bJvfTI130_assertion SIO_000772 10581036 NP508.RA06ck0MWmeMR9GodMpYsCVAlwORnoBhq1n9ie9bJvfTI130_provenance.
- NP508.RA06ck0MWmeMR9GodMpYsCVAlwORnoBhq1n9ie9bJvfTI130_assertion wasDerivedFrom uniprot-2016 NP508.RA06ck0MWmeMR9GodMpYsCVAlwORnoBhq1n9ie9bJvfTI130_provenance.
- NP508.RA06ck0MWmeMR9GodMpYsCVAlwORnoBhq1n9ie9bJvfTI130_assertion wasGeneratedBy ECO_0000218 NP508.RA06ck0MWmeMR9GodMpYsCVAlwORnoBhq1n9ie9bJvfTI130_provenance.