Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP434491.RAK04XlWiVR_-V2LOqT8cPiijze9aPvt_tggVpJB3m8Hg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP434491.RAK04XlWiVR_-V2LOqT8cPiijze9aPvt_tggVpJB3m8Hg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP434491.RAK04XlWiVR_-V2LOqT8cPiijze9aPvt_tggVpJB3m8Hg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP434491.RAK04XlWiVR_-V2LOqT8cPiijze9aPvt_tggVpJB3m8Hg130_provenance.
- NP434491.RAK04XlWiVR_-V2LOqT8cPiijze9aPvt_tggVpJB3m8Hg130_assertion description "[The identification of GRIN2A as a major gene for these epileptic encephalopathies provides crucial insights into the underlying pathophysiology.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP434491.RAK04XlWiVR_-V2LOqT8cPiijze9aPvt_tggVpJB3m8Hg130_provenance.
- NP434491.RAK04XlWiVR_-V2LOqT8cPiijze9aPvt_tggVpJB3m8Hg130_assertion evidence source_evidence_literature NP434491.RAK04XlWiVR_-V2LOqT8cPiijze9aPvt_tggVpJB3m8Hg130_provenance.
- NP434491.RAK04XlWiVR_-V2LOqT8cPiijze9aPvt_tggVpJB3m8Hg130_assertion SIO_000772 23933820 NP434491.RAK04XlWiVR_-V2LOqT8cPiijze9aPvt_tggVpJB3m8Hg130_provenance.
- NP434491.RAK04XlWiVR_-V2LOqT8cPiijze9aPvt_tggVpJB3m8Hg130_assertion wasDerivedFrom befree-20150227 NP434491.RAK04XlWiVR_-V2LOqT8cPiijze9aPvt_tggVpJB3m8Hg130_provenance.
- NP434491.RAK04XlWiVR_-V2LOqT8cPiijze9aPvt_tggVpJB3m8Hg130_assertion wasGeneratedBy ECO_0000203 NP434491.RAK04XlWiVR_-V2LOqT8cPiijze9aPvt_tggVpJB3m8Hg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP434491.RAK04XlWiVR_-V2LOqT8cPiijze9aPvt_tggVpJB3m8Hg130_provenance.