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- NP996645.RAhhJ2xd10M3A90bndt4O9DTw5YTr7CLUlaz_WlYXn97c130_assertion type Assertion NP996645.RAhhJ2xd10M3A90bndt4O9DTw5YTr7CLUlaz_WlYXn97c130_head.
- NP996645.RAhhJ2xd10M3A90bndt4O9DTw5YTr7CLUlaz_WlYXn97c130_assertion wasGeneratedBy ECO_0000203 NP996645.RAhhJ2xd10M3A90bndt4O9DTw5YTr7CLUlaz_WlYXn97c130_provenance.
- NP996645.RAhhJ2xd10M3A90bndt4O9DTw5YTr7CLUlaz_WlYXn97c130_assertion wasDerivedFrom befree-2016 NP996645.RAhhJ2xd10M3A90bndt4O9DTw5YTr7CLUlaz_WlYXn97c130_provenance.
- NP996645.RAhhJ2xd10M3A90bndt4O9DTw5YTr7CLUlaz_WlYXn97c130_assertion SIO_000772 22784463 NP996645.RAhhJ2xd10M3A90bndt4O9DTw5YTr7CLUlaz_WlYXn97c130_provenance.
- NP996645.RAhhJ2xd10M3A90bndt4O9DTw5YTr7CLUlaz_WlYXn97c130_assertion evidence source_evidence_literature NP996645.RAhhJ2xd10M3A90bndt4O9DTw5YTr7CLUlaz_WlYXn97c130_provenance.
- NP996645.RAhhJ2xd10M3A90bndt4O9DTw5YTr7CLUlaz_WlYXn97c130_assertion description "[Clinical and genetic analysis of a compound heterozygous mutation in the thyroglobulin gene in a Chinese twin family with congenital goiter and hypothyroidism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP996645.RAhhJ2xd10M3A90bndt4O9DTw5YTr7CLUlaz_WlYXn97c130_provenance.