Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP559171.RAU8Eiu10QTRzbpz0gVqBp_467QVCPpFGcNDW-H8y2Myo130_assertion> ?p ?o ?g. }
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- NP559171.RAU8Eiu10QTRzbpz0gVqBp_467QVCPpFGcNDW-H8y2Myo130_assertion type Assertion NP559171.RAU8Eiu10QTRzbpz0gVqBp_467QVCPpFGcNDW-H8y2Myo130_head.
- NP559171.RAU8Eiu10QTRzbpz0gVqBp_467QVCPpFGcNDW-H8y2Myo130_assertion description "[Screening all exons of CPA6 in unrelated patients with partial epilepsy (n = 195) and FS (n = 145) revealed a new heterozygous missense mutation c.799G>A (p.Gly267Arg) in three TLE patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP559171.RAU8Eiu10QTRzbpz0gVqBp_467QVCPpFGcNDW-H8y2Myo130_provenance.
- NP559171.RAU8Eiu10QTRzbpz0gVqBp_467QVCPpFGcNDW-H8y2Myo130_assertion evidence source_evidence_literature NP559171.RAU8Eiu10QTRzbpz0gVqBp_467QVCPpFGcNDW-H8y2Myo130_provenance.
- NP559171.RAU8Eiu10QTRzbpz0gVqBp_467QVCPpFGcNDW-H8y2Myo130_assertion SIO_000772 21922598 NP559171.RAU8Eiu10QTRzbpz0gVqBp_467QVCPpFGcNDW-H8y2Myo130_provenance.
- NP559171.RAU8Eiu10QTRzbpz0gVqBp_467QVCPpFGcNDW-H8y2Myo130_assertion wasDerivedFrom befree-20140225 NP559171.RAU8Eiu10QTRzbpz0gVqBp_467QVCPpFGcNDW-H8y2Myo130_provenance.
- NP559171.RAU8Eiu10QTRzbpz0gVqBp_467QVCPpFGcNDW-H8y2Myo130_assertion wasGeneratedBy ECO_0000203 NP559171.RAU8Eiu10QTRzbpz0gVqBp_467QVCPpFGcNDW-H8y2Myo130_provenance.