Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1051376.RA7qSTl9z8ynDISeo_p7512iQVdvA_a6Hvz36VzvHkd84130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1051376.RA7qSTl9z8ynDISeo_p7512iQVdvA_a6Hvz36VzvHkd84130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1051376.RA7qSTl9z8ynDISeo_p7512iQVdvA_a6Hvz36VzvHkd84130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1051376.RA7qSTl9z8ynDISeo_p7512iQVdvA_a6Hvz36VzvHkd84130_provenance.
- NP1051376.RA7qSTl9z8ynDISeo_p7512iQVdvA_a6Hvz36VzvHkd84130_assertion description "[Mutations in ATP13A2 (PARK9), encoding a lysosomal P-type ATPase, are associated with both Kufor-Rakeb syndrome (KRS) and neuronal ceroid lipofuscinosis (NCL).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1051376.RA7qSTl9z8ynDISeo_p7512iQVdvA_a6Hvz36VzvHkd84130_provenance.
- NP1051376.RA7qSTl9z8ynDISeo_p7512iQVdvA_a6Hvz36VzvHkd84130_assertion evidence source_evidence_literature NP1051376.RA7qSTl9z8ynDISeo_p7512iQVdvA_a6Hvz36VzvHkd84130_provenance.
- NP1051376.RA7qSTl9z8ynDISeo_p7512iQVdvA_a6Hvz36VzvHkd84130_assertion SIO_000772 23393156 NP1051376.RA7qSTl9z8ynDISeo_p7512iQVdvA_a6Hvz36VzvHkd84130_provenance.
- NP1051376.RA7qSTl9z8ynDISeo_p7512iQVdvA_a6Hvz36VzvHkd84130_assertion wasDerivedFrom befree-2016 NP1051376.RA7qSTl9z8ynDISeo_p7512iQVdvA_a6Hvz36VzvHkd84130_provenance.
- NP1051376.RA7qSTl9z8ynDISeo_p7512iQVdvA_a6Hvz36VzvHkd84130_assertion wasGeneratedBy ECO_0000203 NP1051376.RA7qSTl9z8ynDISeo_p7512iQVdvA_a6Hvz36VzvHkd84130_provenance.
- befree-2016 importedOn "2016-02-19" NP1051376.RA7qSTl9z8ynDISeo_p7512iQVdvA_a6Hvz36VzvHkd84130_provenance.