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- NP761347.RAHd-_uAkWjcXFilHq9ccA2qcEsXWM-iENlxrO1jUDQ6c130_assertion type Assertion NP761347.RAHd-_uAkWjcXFilHq9ccA2qcEsXWM-iENlxrO1jUDQ6c130_head.
- NP761347.RAHd-_uAkWjcXFilHq9ccA2qcEsXWM-iENlxrO1jUDQ6c130_assertion description "[We also identified a novel homozygous null PUS1 mutation and novel mitochondrial DNA deletions in two patients with Pearson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761347.RAHd-_uAkWjcXFilHq9ccA2qcEsXWM-iENlxrO1jUDQ6c130_provenance.
- NP761347.RAHd-_uAkWjcXFilHq9ccA2qcEsXWM-iENlxrO1jUDQ6c130_assertion evidence source_evidence_literature NP761347.RAHd-_uAkWjcXFilHq9ccA2qcEsXWM-iENlxrO1jUDQ6c130_provenance.
- NP761347.RAHd-_uAkWjcXFilHq9ccA2qcEsXWM-iENlxrO1jUDQ6c130_assertion SIO_000772 19731322 NP761347.RAHd-_uAkWjcXFilHq9ccA2qcEsXWM-iENlxrO1jUDQ6c130_provenance.
- NP761347.RAHd-_uAkWjcXFilHq9ccA2qcEsXWM-iENlxrO1jUDQ6c130_assertion wasDerivedFrom befree-2016 NP761347.RAHd-_uAkWjcXFilHq9ccA2qcEsXWM-iENlxrO1jUDQ6c130_provenance.
- NP761347.RAHd-_uAkWjcXFilHq9ccA2qcEsXWM-iENlxrO1jUDQ6c130_assertion wasGeneratedBy ECO_0000203 NP761347.RAHd-_uAkWjcXFilHq9ccA2qcEsXWM-iENlxrO1jUDQ6c130_provenance.