Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP29810.RA6E8wHWQqnetISr5U8HFnV3G3YQ0pa25rL4wJg24QebA130_assertion> ?p ?o ?g. }
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- NP29810.RA6E8wHWQqnetISr5U8HFnV3G3YQ0pa25rL4wJg24QebA130_assertion type Assertion NP29810.RA6E8wHWQqnetISr5U8HFnV3G3YQ0pa25rL4wJg24QebA130_head.
- NP29810.RA6E8wHWQqnetISr5U8HFnV3G3YQ0pa25rL4wJg24QebA130_assertion description "[The H723R mutation in the PDS/SLC26A4 gene is associated with typical Pendred syndrome in Korean patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP29810.RA6E8wHWQqnetISr5U8HFnV3G3YQ0pa25rL4wJg24QebA130_provenance.
- NP29810.RA6E8wHWQqnetISr5U8HFnV3G3YQ0pa25rL4wJg24QebA130_assertion evidence source_evidence_curated NP29810.RA6E8wHWQqnetISr5U8HFnV3G3YQ0pa25rL4wJg24QebA130_provenance.
- NP29810.RA6E8wHWQqnetISr5U8HFnV3G3YQ0pa25rL4wJg24QebA130_assertion SIO_000772 17322586 NP29810.RA6E8wHWQqnetISr5U8HFnV3G3YQ0pa25rL4wJg24QebA130_provenance.
- NP29810.RA6E8wHWQqnetISr5U8HFnV3G3YQ0pa25rL4wJg24QebA130_assertion wasDerivedFrom ctd_human-20130708 NP29810.RA6E8wHWQqnetISr5U8HFnV3G3YQ0pa25rL4wJg24QebA130_provenance.
- NP29810.RA6E8wHWQqnetISr5U8HFnV3G3YQ0pa25rL4wJg24QebA130_assertion wasGeneratedBy ECO_0000218 NP29810.RA6E8wHWQqnetISr5U8HFnV3G3YQ0pa25rL4wJg24QebA130_provenance.