Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_provenance.
- NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_assertion description "[We have analysed the frequency of PRRT2 mutations in families with benign familial infantile convulsions without paroxysmal kinesigenic dyskinesia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_provenance.
- NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_assertion evidence source_evidence_literature NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_provenance.
- NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_assertion SIO_000772 22877996 NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_provenance.
- NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_assertion wasDerivedFrom befree-2016 NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_provenance.
- NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_assertion wasGeneratedBy ECO_0000203 NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_provenance.