Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682447.RA6ed25W1C6Mbj__OoXSzxwz8tjWuTG8BAAmnmCF15jVQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682447.RA6ed25W1C6Mbj__OoXSzxwz8tjWuTG8BAAmnmCF15jVQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682447.RA6ed25W1C6Mbj__OoXSzxwz8tjWuTG8BAAmnmCF15jVQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682447.RA6ed25W1C6Mbj__OoXSzxwz8tjWuTG8BAAmnmCF15jVQ130_provenance.
- NP682447.RA6ed25W1C6Mbj__OoXSzxwz8tjWuTG8BAAmnmCF15jVQ130_assertion description "[Knowledge of an expanded spectrum of epileptic encephalopathies associated with SCN1A mutations allows earlier diagnostic confirmation for children with these devastating disorders.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682447.RA6ed25W1C6Mbj__OoXSzxwz8tjWuTG8BAAmnmCF15jVQ130_provenance.
- NP682447.RA6ed25W1C6Mbj__OoXSzxwz8tjWuTG8BAAmnmCF15jVQ130_assertion evidence source_evidence_literature NP682447.RA6ed25W1C6Mbj__OoXSzxwz8tjWuTG8BAAmnmCF15jVQ130_provenance.
- NP682447.RA6ed25W1C6Mbj__OoXSzxwz8tjWuTG8BAAmnmCF15jVQ130_assertion SIO_000772 17347258 NP682447.RA6ed25W1C6Mbj__OoXSzxwz8tjWuTG8BAAmnmCF15jVQ130_provenance.
- NP682447.RA6ed25W1C6Mbj__OoXSzxwz8tjWuTG8BAAmnmCF15jVQ130_assertion wasDerivedFrom befree-20150227 NP682447.RA6ed25W1C6Mbj__OoXSzxwz8tjWuTG8BAAmnmCF15jVQ130_provenance.
- NP682447.RA6ed25W1C6Mbj__OoXSzxwz8tjWuTG8BAAmnmCF15jVQ130_assertion wasGeneratedBy ECO_0000203 NP682447.RA6ed25W1C6Mbj__OoXSzxwz8tjWuTG8BAAmnmCF15jVQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682447.RA6ed25W1C6Mbj__OoXSzxwz8tjWuTG8BAAmnmCF15jVQ130_provenance.