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- NP204275.RAdiYdxxHZ-qU0LHOu1L4vWI4bJ-iZjJV29Cq2oCplhqI130_assertion type Assertion NP204275.RAdiYdxxHZ-qU0LHOu1L4vWI4bJ-iZjJV29Cq2oCplhqI130_head.
- NP204275.RAdiYdxxHZ-qU0LHOu1L4vWI4bJ-iZjJV29Cq2oCplhqI130_assertion description "[Biallelic mutations in the NIS gene lead to a congenital iodide transport defect, an autosomal recessive condition characterized by hypothyroidism, goiter, low thyroid iodide uptake, and a low saliva/plasma iodide ratio.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP204275.RAdiYdxxHZ-qU0LHOu1L4vWI4bJ-iZjJV29Cq2oCplhqI130_provenance.
- NP204275.RAdiYdxxHZ-qU0LHOu1L4vWI4bJ-iZjJV29Cq2oCplhqI130_assertion evidence source_evidence_literature NP204275.RAdiYdxxHZ-qU0LHOu1L4vWI4bJ-iZjJV29Cq2oCplhqI130_provenance.
- NP204275.RAdiYdxxHZ-qU0LHOu1L4vWI4bJ-iZjJV29Cq2oCplhqI130_assertion SIO_000772 19196800 NP204275.RAdiYdxxHZ-qU0LHOu1L4vWI4bJ-iZjJV29Cq2oCplhqI130_provenance.
- NP204275.RAdiYdxxHZ-qU0LHOu1L4vWI4bJ-iZjJV29Cq2oCplhqI130_assertion wasDerivedFrom lhgdn-20090331 NP204275.RAdiYdxxHZ-qU0LHOu1L4vWI4bJ-iZjJV29Cq2oCplhqI130_provenance.
- NP204275.RAdiYdxxHZ-qU0LHOu1L4vWI4bJ-iZjJV29Cq2oCplhqI130_assertion wasGeneratedBy ECO_0000203 NP204275.RAdiYdxxHZ-qU0LHOu1L4vWI4bJ-iZjJV29Cq2oCplhqI130_provenance.