Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682507.RAlgQDyhAsWQpYTCkVGgLjJ3aGKIvyiNyyIpADzfsnjOM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP682507.RAlgQDyhAsWQpYTCkVGgLjJ3aGKIvyiNyyIpADzfsnjOM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682507.RAlgQDyhAsWQpYTCkVGgLjJ3aGKIvyiNyyIpADzfsnjOM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682507.RAlgQDyhAsWQpYTCkVGgLjJ3aGKIvyiNyyIpADzfsnjOM130_provenance.
- NP682507.RAlgQDyhAsWQpYTCkVGgLjJ3aGKIvyiNyyIpADzfsnjOM130_assertion description "[These findings confirm that mutations in the SCN1A gene are mainly involved in the pathogenesis of SMEI, rarely in that of SIGEI, and are commonly not found in patients with MAE.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682507.RAlgQDyhAsWQpYTCkVGgLjJ3aGKIvyiNyyIpADzfsnjOM130_provenance.
- NP682507.RAlgQDyhAsWQpYTCkVGgLjJ3aGKIvyiNyyIpADzfsnjOM130_assertion evidence source_evidence_literature NP682507.RAlgQDyhAsWQpYTCkVGgLjJ3aGKIvyiNyyIpADzfsnjOM130_provenance.
- NP682507.RAlgQDyhAsWQpYTCkVGgLjJ3aGKIvyiNyyIpADzfsnjOM130_assertion SIO_000772 19464834 NP682507.RAlgQDyhAsWQpYTCkVGgLjJ3aGKIvyiNyyIpADzfsnjOM130_provenance.
- NP682507.RAlgQDyhAsWQpYTCkVGgLjJ3aGKIvyiNyyIpADzfsnjOM130_assertion wasDerivedFrom befree-20150227 NP682507.RAlgQDyhAsWQpYTCkVGgLjJ3aGKIvyiNyyIpADzfsnjOM130_provenance.
- NP682507.RAlgQDyhAsWQpYTCkVGgLjJ3aGKIvyiNyyIpADzfsnjOM130_assertion wasGeneratedBy ECO_0000203 NP682507.RAlgQDyhAsWQpYTCkVGgLjJ3aGKIvyiNyyIpADzfsnjOM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682507.RAlgQDyhAsWQpYTCkVGgLjJ3aGKIvyiNyyIpADzfsnjOM130_provenance.