Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP697675.RAckyP8HXEMGPX0go95eRkgsleotnnTJkukMuEDboXIAY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP697675.RAckyP8HXEMGPX0go95eRkgsleotnnTJkukMuEDboXIAY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP697675.RAckyP8HXEMGPX0go95eRkgsleotnnTJkukMuEDboXIAY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP697675.RAckyP8HXEMGPX0go95eRkgsleotnnTJkukMuEDboXIAY130_provenance.
- NP697675.RAckyP8HXEMGPX0go95eRkgsleotnnTJkukMuEDboXIAY130_assertion description "[This familial case has the characteristic features of myosclerosis myopathy and carries a homozygous COL6A2 mutation responsible for a peculiar pattern of collagen VI defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP697675.RAckyP8HXEMGPX0go95eRkgsleotnnTJkukMuEDboXIAY130_provenance.
- NP697675.RAckyP8HXEMGPX0go95eRkgsleotnnTJkukMuEDboXIAY130_assertion evidence source_evidence_literature NP697675.RAckyP8HXEMGPX0go95eRkgsleotnnTJkukMuEDboXIAY130_provenance.
- NP697675.RAckyP8HXEMGPX0go95eRkgsleotnnTJkukMuEDboXIAY130_assertion SIO_000772 18852439 NP697675.RAckyP8HXEMGPX0go95eRkgsleotnnTJkukMuEDboXIAY130_provenance.
- NP697675.RAckyP8HXEMGPX0go95eRkgsleotnnTJkukMuEDboXIAY130_assertion wasDerivedFrom befree-2016 NP697675.RAckyP8HXEMGPX0go95eRkgsleotnnTJkukMuEDboXIAY130_provenance.
- NP697675.RAckyP8HXEMGPX0go95eRkgsleotnnTJkukMuEDboXIAY130_assertion wasGeneratedBy ECO_0000203 NP697675.RAckyP8HXEMGPX0go95eRkgsleotnnTJkukMuEDboXIAY130_provenance.
- befree-2016 importedOn "2016-02-19" NP697675.RAckyP8HXEMGPX0go95eRkgsleotnnTJkukMuEDboXIAY130_provenance.