Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_provenance.
- NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_assertion description "[Missense mutations of ACTA1 cause an autosomal dominant congenital myopathy with cores.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_provenance.
- NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_assertion evidence source_evidence_literature NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_provenance.
- NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_assertion SIO_000772 15520409 NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_provenance.
- NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_assertion wasDerivedFrom lhgdn-20090331 NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_provenance.
- NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_assertion wasGeneratedBy ECO_0000203 NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP198139.RAa9Hgb9caSiGQx7Gs3cXSwKIqWI_hR-4k59NeCzfI0JI130_provenance.