Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP719363.RAIcDBmCql5dqQSXM-c1qrARbQn3Sz6k9Gw4xjpTcYw9I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP719363.RAIcDBmCql5dqQSXM-c1qrARbQn3Sz6k9Gw4xjpTcYw9I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP719363.RAIcDBmCql5dqQSXM-c1qrARbQn3Sz6k9Gw4xjpTcYw9I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP719363.RAIcDBmCql5dqQSXM-c1qrARbQn3Sz6k9Gw4xjpTcYw9I130_provenance.
- NP719363.RAIcDBmCql5dqQSXM-c1qrARbQn3Sz6k9Gw4xjpTcYw9I130_assertion description "[Mutations in CDKL5 and ARX are known causes of early-onset epilepsy and severe developmental delay in males and females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP719363.RAIcDBmCql5dqQSXM-c1qrARbQn3Sz6k9Gw4xjpTcYw9I130_provenance.
- NP719363.RAIcDBmCql5dqQSXM-c1qrARbQn3Sz6k9Gw4xjpTcYw9I130_assertion evidence source_evidence_literature NP719363.RAIcDBmCql5dqQSXM-c1qrARbQn3Sz6k9Gw4xjpTcYw9I130_provenance.
- NP719363.RAIcDBmCql5dqQSXM-c1qrARbQn3Sz6k9Gw4xjpTcYw9I130_assertion SIO_000772 23583054 NP719363.RAIcDBmCql5dqQSXM-c1qrARbQn3Sz6k9Gw4xjpTcYw9I130_provenance.
- NP719363.RAIcDBmCql5dqQSXM-c1qrARbQn3Sz6k9Gw4xjpTcYw9I130_assertion wasDerivedFrom befree-20150227 NP719363.RAIcDBmCql5dqQSXM-c1qrARbQn3Sz6k9Gw4xjpTcYw9I130_provenance.
- NP719363.RAIcDBmCql5dqQSXM-c1qrARbQn3Sz6k9Gw4xjpTcYw9I130_assertion wasGeneratedBy ECO_0000203 NP719363.RAIcDBmCql5dqQSXM-c1qrARbQn3Sz6k9Gw4xjpTcYw9I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP719363.RAIcDBmCql5dqQSXM-c1qrARbQn3Sz6k9Gw4xjpTcYw9I130_provenance.