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- source_evidence_literature type ECO_0000212 NP682571.RA2AEMGImqm9zVZMO2_fpoTkk-oy6uHqp_cxIVHx4XE8c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682571.RA2AEMGImqm9zVZMO2_fpoTkk-oy6uHqp_cxIVHx4XE8c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682571.RA2AEMGImqm9zVZMO2_fpoTkk-oy6uHqp_cxIVHx4XE8c130_provenance.
- NP682571.RA2AEMGImqm9zVZMO2_fpoTkk-oy6uHqp_cxIVHx4XE8c130_assertion description "[Acute encephalopathy with a truncation mutation in the SCN1A gene: a case report.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682571.RA2AEMGImqm9zVZMO2_fpoTkk-oy6uHqp_cxIVHx4XE8c130_provenance.
- NP682571.RA2AEMGImqm9zVZMO2_fpoTkk-oy6uHqp_cxIVHx4XE8c130_assertion evidence source_evidence_literature NP682571.RA2AEMGImqm9zVZMO2_fpoTkk-oy6uHqp_cxIVHx4XE8c130_provenance.
- NP682571.RA2AEMGImqm9zVZMO2_fpoTkk-oy6uHqp_cxIVHx4XE8c130_assertion SIO_000772 20491869 NP682571.RA2AEMGImqm9zVZMO2_fpoTkk-oy6uHqp_cxIVHx4XE8c130_provenance.
- NP682571.RA2AEMGImqm9zVZMO2_fpoTkk-oy6uHqp_cxIVHx4XE8c130_assertion wasDerivedFrom befree-20150227 NP682571.RA2AEMGImqm9zVZMO2_fpoTkk-oy6uHqp_cxIVHx4XE8c130_provenance.
- NP682571.RA2AEMGImqm9zVZMO2_fpoTkk-oy6uHqp_cxIVHx4XE8c130_assertion wasGeneratedBy ECO_0000203 NP682571.RA2AEMGImqm9zVZMO2_fpoTkk-oy6uHqp_cxIVHx4XE8c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP682571.RA2AEMGImqm9zVZMO2_fpoTkk-oy6uHqp_cxIVHx4XE8c130_provenance.