Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_assertion> ?p ?o ?g. }
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- NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_assertion type Assertion NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_head.
- NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_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." NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_provenance.
- NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_assertion evidence source_evidence_literature NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_provenance.
- NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_assertion SIO_000772 16684826 NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_provenance.
- NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_assertion wasDerivedFrom befree-20140225 NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_provenance.
- NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_assertion wasGeneratedBy ECO_0000203 NP268624.RADhTs2gtpXGGCoViYsvt_WiqyJ_7li55H3MViWz0bInI130_provenance.