Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP285516.RA7gqxXtIHiWlJ9t2_Y3zIwYkzEcCa9whaaSDTqoGV6mo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP285516.RA7gqxXtIHiWlJ9t2_Y3zIwYkzEcCa9whaaSDTqoGV6mo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP285516.RA7gqxXtIHiWlJ9t2_Y3zIwYkzEcCa9whaaSDTqoGV6mo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP285516.RA7gqxXtIHiWlJ9t2_Y3zIwYkzEcCa9whaaSDTqoGV6mo130_provenance.
- NP285516.RA7gqxXtIHiWlJ9t2_Y3zIwYkzEcCa9whaaSDTqoGV6mo130_assertion description "[These include lamin A/C in autosomal dominant Emery-Dreifuss muscular dystrophy, SMN in spinal muscular atrophy, SIX5 in myotonic dystrophy, calpain3 in type 2A limb-girdle muscular dystrophy, PABP2 in oculopharyngeal dystrophy, androgen receptor in spinal and bulbar muscular atrophy and the ataxins in hereditary ataxias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285516.RA7gqxXtIHiWlJ9t2_Y3zIwYkzEcCa9whaaSDTqoGV6mo130_provenance.
- NP285516.RA7gqxXtIHiWlJ9t2_Y3zIwYkzEcCa9whaaSDTqoGV6mo130_assertion evidence source_evidence_literature NP285516.RA7gqxXtIHiWlJ9t2_Y3zIwYkzEcCa9whaaSDTqoGV6mo130_provenance.
- NP285516.RA7gqxXtIHiWlJ9t2_Y3zIwYkzEcCa9whaaSDTqoGV6mo130_assertion SIO_000772 10838245 NP285516.RA7gqxXtIHiWlJ9t2_Y3zIwYkzEcCa9whaaSDTqoGV6mo130_provenance.
- NP285516.RA7gqxXtIHiWlJ9t2_Y3zIwYkzEcCa9whaaSDTqoGV6mo130_assertion wasDerivedFrom befree-2016 NP285516.RA7gqxXtIHiWlJ9t2_Y3zIwYkzEcCa9whaaSDTqoGV6mo130_provenance.
- NP285516.RA7gqxXtIHiWlJ9t2_Y3zIwYkzEcCa9whaaSDTqoGV6mo130_assertion wasGeneratedBy ECO_0000203 NP285516.RA7gqxXtIHiWlJ9t2_Y3zIwYkzEcCa9whaaSDTqoGV6mo130_provenance.
- befree-2016 importedOn "2016-02-19" NP285516.RA7gqxXtIHiWlJ9t2_Y3zIwYkzEcCa9whaaSDTqoGV6mo130_provenance.