Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP7991.RATcTc1giLeaGi7EMQ8JQJe-pIAnjrQwwhbw9XFYoNJ5E130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP7991.RATcTc1giLeaGi7EMQ8JQJe-pIAnjrQwwhbw9XFYoNJ5E130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP7991.RATcTc1giLeaGi7EMQ8JQJe-pIAnjrQwwhbw9XFYoNJ5E130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP7991.RATcTc1giLeaGi7EMQ8JQJe-pIAnjrQwwhbw9XFYoNJ5E130_provenance.
- NP7991.RATcTc1giLeaGi7EMQ8JQJe-pIAnjrQwwhbw9XFYoNJ5E130_assertion description "[Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7991.RATcTc1giLeaGi7EMQ8JQJe-pIAnjrQwwhbw9XFYoNJ5E130_provenance.
- NP7991.RATcTc1giLeaGi7EMQ8JQJe-pIAnjrQwwhbw9XFYoNJ5E130_assertion evidence source_evidence_curated NP7991.RATcTc1giLeaGi7EMQ8JQJe-pIAnjrQwwhbw9XFYoNJ5E130_provenance.
- NP7991.RATcTc1giLeaGi7EMQ8JQJe-pIAnjrQwwhbw9XFYoNJ5E130_assertion SIO_000772 25155093 NP7991.RATcTc1giLeaGi7EMQ8JQJe-pIAnjrQwwhbw9XFYoNJ5E130_provenance.
- NP7991.RATcTc1giLeaGi7EMQ8JQJe-pIAnjrQwwhbw9XFYoNJ5E130_assertion wasDerivedFrom uniprot-2016 NP7991.RATcTc1giLeaGi7EMQ8JQJe-pIAnjrQwwhbw9XFYoNJ5E130_provenance.
- NP7991.RATcTc1giLeaGi7EMQ8JQJe-pIAnjrQwwhbw9XFYoNJ5E130_assertion wasGeneratedBy ECO_0000218 NP7991.RATcTc1giLeaGi7EMQ8JQJe-pIAnjrQwwhbw9XFYoNJ5E130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP7991.RATcTc1giLeaGi7EMQ8JQJe-pIAnjrQwwhbw9XFYoNJ5E130_provenance.