Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP418998.RAEABmcn7Pt9Ug6Weeju7vev0KkRJw82nDhDmJTlqXySI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP418998.RAEABmcn7Pt9Ug6Weeju7vev0KkRJw82nDhDmJTlqXySI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418998.RAEABmcn7Pt9Ug6Weeju7vev0KkRJw82nDhDmJTlqXySI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418998.RAEABmcn7Pt9Ug6Weeju7vev0KkRJw82nDhDmJTlqXySI130_provenance.
- NP418998.RAEABmcn7Pt9Ug6Weeju7vev0KkRJw82nDhDmJTlqXySI130_assertion description "[In analogy to symptomatic female dystrophinopathy carriers, our results suggest that heterozygous alpha-sarcoglycan gene mutation carriers can be symptomatic with selective muscle weakness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418998.RAEABmcn7Pt9Ug6Weeju7vev0KkRJw82nDhDmJTlqXySI130_provenance.
- NP418998.RAEABmcn7Pt9Ug6Weeju7vev0KkRJw82nDhDmJTlqXySI130_assertion evidence source_evidence_literature NP418998.RAEABmcn7Pt9Ug6Weeju7vev0KkRJw82nDhDmJTlqXySI130_provenance.
- NP418998.RAEABmcn7Pt9Ug6Weeju7vev0KkRJw82nDhDmJTlqXySI130_assertion SIO_000772 14595658 NP418998.RAEABmcn7Pt9Ug6Weeju7vev0KkRJw82nDhDmJTlqXySI130_provenance.
- NP418998.RAEABmcn7Pt9Ug6Weeju7vev0KkRJw82nDhDmJTlqXySI130_assertion wasDerivedFrom befree-2016 NP418998.RAEABmcn7Pt9Ug6Weeju7vev0KkRJw82nDhDmJTlqXySI130_provenance.
- NP418998.RAEABmcn7Pt9Ug6Weeju7vev0KkRJw82nDhDmJTlqXySI130_assertion wasGeneratedBy ECO_0000203 NP418998.RAEABmcn7Pt9Ug6Weeju7vev0KkRJw82nDhDmJTlqXySI130_provenance.
- befree-2016 importedOn "2016-02-19" NP418998.RAEABmcn7Pt9Ug6Weeju7vev0KkRJw82nDhDmJTlqXySI130_provenance.