Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1219855.RA1v7jwH_sYHa7bO2bO-gqDz2vOfaev0cMb3wDZDyrt6M130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1219855.RA1v7jwH_sYHa7bO2bO-gqDz2vOfaev0cMb3wDZDyrt6M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1219855.RA1v7jwH_sYHa7bO2bO-gqDz2vOfaev0cMb3wDZDyrt6M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1219855.RA1v7jwH_sYHa7bO2bO-gqDz2vOfaev0cMb3wDZDyrt6M130_provenance.
- befree-2016 importedOn "2016-02-19" NP1219855.RA1v7jwH_sYHa7bO2bO-gqDz2vOfaev0cMb3wDZDyrt6M130_provenance.
- NP1219855.RA1v7jwH_sYHa7bO2bO-gqDz2vOfaev0cMb3wDZDyrt6M130_assertion wasGeneratedBy ECO_0000203 NP1219855.RA1v7jwH_sYHa7bO2bO-gqDz2vOfaev0cMb3wDZDyrt6M130_provenance.
- NP1219855.RA1v7jwH_sYHa7bO2bO-gqDz2vOfaev0cMb3wDZDyrt6M130_assertion wasDerivedFrom befree-2016 NP1219855.RA1v7jwH_sYHa7bO2bO-gqDz2vOfaev0cMb3wDZDyrt6M130_provenance.
- NP1219855.RA1v7jwH_sYHa7bO2bO-gqDz2vOfaev0cMb3wDZDyrt6M130_assertion SIO_000772 25218114 NP1219855.RA1v7jwH_sYHa7bO2bO-gqDz2vOfaev0cMb3wDZDyrt6M130_provenance.
- NP1219855.RA1v7jwH_sYHa7bO2bO-gqDz2vOfaev0cMb3wDZDyrt6M130_assertion evidence source_evidence_literature NP1219855.RA1v7jwH_sYHa7bO2bO-gqDz2vOfaev0cMb3wDZDyrt6M130_provenance.
- NP1219855.RA1v7jwH_sYHa7bO2bO-gqDz2vOfaev0cMb3wDZDyrt6M130_assertion description "[Direct sequencing of PCDH19 gene was conducted in 31 unrelated female patients with early onset (<1 year of age) epilepsy and a wide spectrum of phenotypes including febrile seizures, focal and generalized forms, with either sporadic or familial distribution.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1219855.RA1v7jwH_sYHa7bO2bO-gqDz2vOfaev0cMb3wDZDyrt6M130_provenance.