Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_assertion> ?p ?o ?g. }
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- NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_assertion type Assertion NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_head.
- NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_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." NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_provenance.
- NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_assertion evidence source_evidence_literature NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_provenance.
- NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_assertion SIO_000772 16684826 NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_provenance.
- NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_assertion wasDerivedFrom befree-2016 NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_provenance.
- NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_assertion wasGeneratedBy ECO_0000203 NP548855.RA1sS4dzDKyZbjnwa6NWxxcl9FWT6LeVf497srx0XmtTY130_provenance.