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- NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_assertion type Assertion NP1003935.RAoyahBOqKeL6naILHA4Dr2pCkxFrTZaRsibOHmyh8_JQ130_head.
- 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.