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- source_evidence_literature type ECO_0000212 NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_provenance.
- NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_assertion description "[Limb-girdle muscular dystrophy type 2A (LGMD2A) due to mutations in the CAPN3 gene is one of the most common of autosomal recessive limb-girdle muscular dystrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_provenance.
- NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_assertion evidence source_evidence_literature NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_provenance.
- NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_assertion SIO_000772 24715573 NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_provenance.
- NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_assertion wasDerivedFrom befree-20150227 NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_provenance.
- NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_assertion wasGeneratedBy ECO_0000203 NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_provenance.
- befree-20150227 importedOn "2015-02-27" NP280371.RAVjqJpAd9GwJEYEZCLh1_Z_ct27qUo3bqP37McEj15Us130_provenance.