Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_assertion> ?p ?o ?g. }
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- NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_assertion type Assertion NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_head.
- NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_assertion description "[Our study illustrates that if only a single heterozygous SLC26A4/PDS mutation is found in a patient with goiter and deafness, other genetic explanations should be considered.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_provenance.
- NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_assertion evidence source_evidence_literature NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_provenance.
- NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_assertion SIO_000772 16684826 NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_provenance.
- NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_assertion wasDerivedFrom befree-20140225 NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_provenance.
- NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_assertion wasGeneratedBy ECO_0000203 NP691316.RA886uIO4AGna2WuvV8gACM_QtJdkybDngcDBm4CsU4dM130_provenance.