Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1244142.RAovP7oicO28tN7J-oaR-VMayWNGPYnJVo-6jG-RmdOXs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1244142.RAovP7oicO28tN7J-oaR-VMayWNGPYnJVo-6jG-RmdOXs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1244142.RAovP7oicO28tN7J-oaR-VMayWNGPYnJVo-6jG-RmdOXs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1244142.RAovP7oicO28tN7J-oaR-VMayWNGPYnJVo-6jG-RmdOXs130_provenance.
- NP1244142.RAovP7oicO28tN7J-oaR-VMayWNGPYnJVo-6jG-RmdOXs130_assertion description "[The phenotypic spectrum of C9ORF72 hexanucleotide repeat expansion mutation has been reported to include parkinsonian syndrome, Huntington's disease-like syndrome and dementia syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244142.RAovP7oicO28tN7J-oaR-VMayWNGPYnJVo-6jG-RmdOXs130_provenance.
- NP1244142.RAovP7oicO28tN7J-oaR-VMayWNGPYnJVo-6jG-RmdOXs130_assertion evidence source_evidence_literature NP1244142.RAovP7oicO28tN7J-oaR-VMayWNGPYnJVo-6jG-RmdOXs130_provenance.
- NP1244142.RAovP7oicO28tN7J-oaR-VMayWNGPYnJVo-6jG-RmdOXs130_assertion SIO_000772 25467142 NP1244142.RAovP7oicO28tN7J-oaR-VMayWNGPYnJVo-6jG-RmdOXs130_provenance.
- NP1244142.RAovP7oicO28tN7J-oaR-VMayWNGPYnJVo-6jG-RmdOXs130_assertion wasDerivedFrom befree-2016 NP1244142.RAovP7oicO28tN7J-oaR-VMayWNGPYnJVo-6jG-RmdOXs130_provenance.
- NP1244142.RAovP7oicO28tN7J-oaR-VMayWNGPYnJVo-6jG-RmdOXs130_assertion wasGeneratedBy ECO_0000203 NP1244142.RAovP7oicO28tN7J-oaR-VMayWNGPYnJVo-6jG-RmdOXs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1244142.RAovP7oicO28tN7J-oaR-VMayWNGPYnJVo-6jG-RmdOXs130_provenance.