Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP761347.RAHd-_uAkWjcXFilHq9ccA2qcEsXWM-iENlxrO1jUDQ6c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP761347.RAHd-_uAkWjcXFilHq9ccA2qcEsXWM-iENlxrO1jUDQ6c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP761347.RAHd-_uAkWjcXFilHq9ccA2qcEsXWM-iENlxrO1jUDQ6c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP761347.RAHd-_uAkWjcXFilHq9ccA2qcEsXWM-iENlxrO1jUDQ6c130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP761347.RAHd-_uAkWjcXFilHq9ccA2qcEsXWM-iENlxrO1jUDQ6c130_provenance.