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- NP164319.RADly73OLXmdsuNBmirUwur9NdA__i5vqiGgnTxrfnl6I130_assertion type Assertion NP164319.RADly73OLXmdsuNBmirUwur9NdA__i5vqiGgnTxrfnl6I130_head.
- NP164319.RADly73OLXmdsuNBmirUwur9NdA__i5vqiGgnTxrfnl6I130_assertion description "[An A8296G mutation in the MT-TK gene of a patient with epilepsy - a disease-causing mutation or rare polymorphism?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP164319.RADly73OLXmdsuNBmirUwur9NdA__i5vqiGgnTxrfnl6I130_provenance.
- NP164319.RADly73OLXmdsuNBmirUwur9NdA__i5vqiGgnTxrfnl6I130_assertion evidence source_evidence_literature NP164319.RADly73OLXmdsuNBmirUwur9NdA__i5vqiGgnTxrfnl6I130_provenance.
- NP164319.RADly73OLXmdsuNBmirUwur9NdA__i5vqiGgnTxrfnl6I130_assertion SIO_000772 18651333 NP164319.RADly73OLXmdsuNBmirUwur9NdA__i5vqiGgnTxrfnl6I130_provenance.
- NP164319.RADly73OLXmdsuNBmirUwur9NdA__i5vqiGgnTxrfnl6I130_assertion wasDerivedFrom befree-20140225 NP164319.RADly73OLXmdsuNBmirUwur9NdA__i5vqiGgnTxrfnl6I130_provenance.
- NP164319.RADly73OLXmdsuNBmirUwur9NdA__i5vqiGgnTxrfnl6I130_assertion wasGeneratedBy ECO_0000203 NP164319.RADly73OLXmdsuNBmirUwur9NdA__i5vqiGgnTxrfnl6I130_provenance.