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- source_evidence_literature type ECO_0000212 NP1188066.RAdAoxfV2LfO_1zBe8MHJITQifwizL8Jnj6YCea49ES8c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1188066.RAdAoxfV2LfO_1zBe8MHJITQifwizL8Jnj6YCea49ES8c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1188066.RAdAoxfV2LfO_1zBe8MHJITQifwizL8Jnj6YCea49ES8c130_provenance.
- NP1188066.RAdAoxfV2LfO_1zBe8MHJITQifwizL8Jnj6YCea49ES8c130_assertion description "[De novo SCN8A mutations have been reported in patients with epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1188066.RAdAoxfV2LfO_1zBe8MHJITQifwizL8Jnj6YCea49ES8c130_provenance.
- NP1188066.RAdAoxfV2LfO_1zBe8MHJITQifwizL8Jnj6YCea49ES8c130_assertion evidence source_evidence_literature NP1188066.RAdAoxfV2LfO_1zBe8MHJITQifwizL8Jnj6YCea49ES8c130_provenance.
- NP1188066.RAdAoxfV2LfO_1zBe8MHJITQifwizL8Jnj6YCea49ES8c130_assertion SIO_000772 24888894 NP1188066.RAdAoxfV2LfO_1zBe8MHJITQifwizL8Jnj6YCea49ES8c130_provenance.
- NP1188066.RAdAoxfV2LfO_1zBe8MHJITQifwizL8Jnj6YCea49ES8c130_assertion wasDerivedFrom befree-2016 NP1188066.RAdAoxfV2LfO_1zBe8MHJITQifwizL8Jnj6YCea49ES8c130_provenance.
- NP1188066.RAdAoxfV2LfO_1zBe8MHJITQifwizL8Jnj6YCea49ES8c130_assertion wasGeneratedBy ECO_0000203 NP1188066.RAdAoxfV2LfO_1zBe8MHJITQifwizL8Jnj6YCea49ES8c130_provenance.
- befree-2016 importedOn "2016-02-19" NP1188066.RAdAoxfV2LfO_1zBe8MHJITQifwizL8Jnj6YCea49ES8c130_provenance.