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- NP730969.RA_jOakApPxmpvOSG6z5JSWkTXk51mARTIrg5iVoPuHYA130_assertion type Assertion NP730969.RA_jOakApPxmpvOSG6z5JSWkTXk51mARTIrg5iVoPuHYA130_head.
- NP730969.RA_jOakApPxmpvOSG6z5JSWkTXk51mARTIrg5iVoPuHYA130_assertion wasGeneratedBy ECO_0000203 NP730969.RA_jOakApPxmpvOSG6z5JSWkTXk51mARTIrg5iVoPuHYA130_provenance.
- NP730969.RA_jOakApPxmpvOSG6z5JSWkTXk51mARTIrg5iVoPuHYA130_assertion wasDerivedFrom befree-20150227 NP730969.RA_jOakApPxmpvOSG6z5JSWkTXk51mARTIrg5iVoPuHYA130_provenance.
- NP730969.RA_jOakApPxmpvOSG6z5JSWkTXk51mARTIrg5iVoPuHYA130_assertion SIO_000772 22784463 NP730969.RA_jOakApPxmpvOSG6z5JSWkTXk51mARTIrg5iVoPuHYA130_provenance.
- NP730969.RA_jOakApPxmpvOSG6z5JSWkTXk51mARTIrg5iVoPuHYA130_assertion evidence source_evidence_literature NP730969.RA_jOakApPxmpvOSG6z5JSWkTXk51mARTIrg5iVoPuHYA130_provenance.
- NP730969.RA_jOakApPxmpvOSG6z5JSWkTXk51mARTIrg5iVoPuHYA130_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." NP730969.RA_jOakApPxmpvOSG6z5JSWkTXk51mARTIrg5iVoPuHYA130_provenance.