Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978092.RANqH1dIMl3OZVkmzf-Nq5lt4LjJ4r_FtWT9VgkPQr7R8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP978092.RANqH1dIMl3OZVkmzf-Nq5lt4LjJ4r_FtWT9VgkPQr7R8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978092.RANqH1dIMl3OZVkmzf-Nq5lt4LjJ4r_FtWT9VgkPQr7R8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978092.RANqH1dIMl3OZVkmzf-Nq5lt4LjJ4r_FtWT9VgkPQr7R8130_provenance.
- NP978092.RANqH1dIMl3OZVkmzf-Nq5lt4LjJ4r_FtWT9VgkPQr7R8130_assertion description "[CDKL5 and ARX mutations in males with early-onset epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978092.RANqH1dIMl3OZVkmzf-Nq5lt4LjJ4r_FtWT9VgkPQr7R8130_provenance.
- NP978092.RANqH1dIMl3OZVkmzf-Nq5lt4LjJ4r_FtWT9VgkPQr7R8130_assertion evidence source_evidence_literature NP978092.RANqH1dIMl3OZVkmzf-Nq5lt4LjJ4r_FtWT9VgkPQr7R8130_provenance.
- NP978092.RANqH1dIMl3OZVkmzf-Nq5lt4LjJ4r_FtWT9VgkPQr7R8130_assertion SIO_000772 23583054 NP978092.RANqH1dIMl3OZVkmzf-Nq5lt4LjJ4r_FtWT9VgkPQr7R8130_provenance.
- NP978092.RANqH1dIMl3OZVkmzf-Nq5lt4LjJ4r_FtWT9VgkPQr7R8130_assertion wasDerivedFrom befree-20150227 NP978092.RANqH1dIMl3OZVkmzf-Nq5lt4LjJ4r_FtWT9VgkPQr7R8130_provenance.
- NP978092.RANqH1dIMl3OZVkmzf-Nq5lt4LjJ4r_FtWT9VgkPQr7R8130_assertion wasGeneratedBy ECO_0000203 NP978092.RANqH1dIMl3OZVkmzf-Nq5lt4LjJ4r_FtWT9VgkPQr7R8130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978092.RANqH1dIMl3OZVkmzf-Nq5lt4LjJ4r_FtWT9VgkPQr7R8130_provenance.