Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP385225.RAJFJmNZ-qPy7UGsv5nMzs5IkbkVgOiKmAOEg2xppLyms130_assertion> ?p ?o ?g. }
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- NP385225.RAJFJmNZ-qPy7UGsv5nMzs5IkbkVgOiKmAOEg2xppLyms130_assertion type Assertion NP385225.RAJFJmNZ-qPy7UGsv5nMzs5IkbkVgOiKmAOEg2xppLyms130_head.
- NP385225.RAJFJmNZ-qPy7UGsv5nMzs5IkbkVgOiKmAOEg2xppLyms130_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." NP385225.RAJFJmNZ-qPy7UGsv5nMzs5IkbkVgOiKmAOEg2xppLyms130_provenance.
- NP385225.RAJFJmNZ-qPy7UGsv5nMzs5IkbkVgOiKmAOEg2xppLyms130_assertion evidence source_evidence_literature NP385225.RAJFJmNZ-qPy7UGsv5nMzs5IkbkVgOiKmAOEg2xppLyms130_provenance.
- NP385225.RAJFJmNZ-qPy7UGsv5nMzs5IkbkVgOiKmAOEg2xppLyms130_assertion SIO_000772 16684826 NP385225.RAJFJmNZ-qPy7UGsv5nMzs5IkbkVgOiKmAOEg2xppLyms130_provenance.
- NP385225.RAJFJmNZ-qPy7UGsv5nMzs5IkbkVgOiKmAOEg2xppLyms130_assertion wasDerivedFrom befree-20140225 NP385225.RAJFJmNZ-qPy7UGsv5nMzs5IkbkVgOiKmAOEg2xppLyms130_provenance.
- NP385225.RAJFJmNZ-qPy7UGsv5nMzs5IkbkVgOiKmAOEg2xppLyms130_assertion wasGeneratedBy ECO_0000203 NP385225.RAJFJmNZ-qPy7UGsv5nMzs5IkbkVgOiKmAOEg2xppLyms130_provenance.