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- source_evidence_literature type ECO_0000212 NP1117075.RAP2FNQDj0G2sBBJdPF5_ZyF8xPQyS0c4MQS-XLS0Bpxs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1117075.RAP2FNQDj0G2sBBJdPF5_ZyF8xPQyS0c4MQS-XLS0Bpxs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1117075.RAP2FNQDj0G2sBBJdPF5_ZyF8xPQyS0c4MQS-XLS0Bpxs130_provenance.
- NP1117075.RAP2FNQDj0G2sBBJdPF5_ZyF8xPQyS0c4MQS-XLS0Bpxs130_assertion description "[PRRT2 mutations do not seem to be involved in the aetiology of FS or infantile epileptic encephalopathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1117075.RAP2FNQDj0G2sBBJdPF5_ZyF8xPQyS0c4MQS-XLS0Bpxs130_provenance.
- NP1117075.RAP2FNQDj0G2sBBJdPF5_ZyF8xPQyS0c4MQS-XLS0Bpxs130_assertion evidence source_evidence_literature NP1117075.RAP2FNQDj0G2sBBJdPF5_ZyF8xPQyS0c4MQS-XLS0Bpxs130_provenance.
- NP1117075.RAP2FNQDj0G2sBBJdPF5_ZyF8xPQyS0c4MQS-XLS0Bpxs130_assertion SIO_000772 24101679 NP1117075.RAP2FNQDj0G2sBBJdPF5_ZyF8xPQyS0c4MQS-XLS0Bpxs130_provenance.
- NP1117075.RAP2FNQDj0G2sBBJdPF5_ZyF8xPQyS0c4MQS-XLS0Bpxs130_assertion wasDerivedFrom befree-2016 NP1117075.RAP2FNQDj0G2sBBJdPF5_ZyF8xPQyS0c4MQS-XLS0Bpxs130_provenance.
- NP1117075.RAP2FNQDj0G2sBBJdPF5_ZyF8xPQyS0c4MQS-XLS0Bpxs130_assertion wasGeneratedBy ECO_0000203 NP1117075.RAP2FNQDj0G2sBBJdPF5_ZyF8xPQyS0c4MQS-XLS0Bpxs130_provenance.
- befree-2016 importedOn "2016-02-19" NP1117075.RAP2FNQDj0G2sBBJdPF5_ZyF8xPQyS0c4MQS-XLS0Bpxs130_provenance.