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- NP1092482.RAGeOBbcFU3bhMryVYYHRxifBIOnJVaR4Fp4lAz_cbI2M130_assertion type Assertion NP1092482.RAGeOBbcFU3bhMryVYYHRxifBIOnJVaR4Fp4lAz_cbI2M130_head.
- NP1092482.RAGeOBbcFU3bhMryVYYHRxifBIOnJVaR4Fp4lAz_cbI2M130_assertion wasGeneratedBy ECO_0000203 NP1092482.RAGeOBbcFU3bhMryVYYHRxifBIOnJVaR4Fp4lAz_cbI2M130_provenance.
- NP1092482.RAGeOBbcFU3bhMryVYYHRxifBIOnJVaR4Fp4lAz_cbI2M130_assertion wasDerivedFrom befree-2016 NP1092482.RAGeOBbcFU3bhMryVYYHRxifBIOnJVaR4Fp4lAz_cbI2M130_provenance.
- NP1092482.RAGeOBbcFU3bhMryVYYHRxifBIOnJVaR4Fp4lAz_cbI2M130_assertion SIO_000772 23838748 NP1092482.RAGeOBbcFU3bhMryVYYHRxifBIOnJVaR4Fp4lAz_cbI2M130_provenance.
- NP1092482.RAGeOBbcFU3bhMryVYYHRxifBIOnJVaR4Fp4lAz_cbI2M130_assertion evidence source_evidence_literature NP1092482.RAGeOBbcFU3bhMryVYYHRxifBIOnJVaR4Fp4lAz_cbI2M130_provenance.
- NP1092482.RAGeOBbcFU3bhMryVYYHRxifBIOnJVaR4Fp4lAz_cbI2M130_assertion description "[We describe a four-generation Italian family with familial hemiplegic migraine (FHM) and epilepsy due to a novel ATP1A2 missense mutation (R1007W).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1092482.RAGeOBbcFU3bhMryVYYHRxifBIOnJVaR4Fp4lAz_cbI2M130_provenance.