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- source_evidence_literature type ECO_0000212 NP540177.RAxgZS3QOcyX_Fp9ZqD7q8QCma0fEyZym8SjkzXdAFX8M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP540177.RAxgZS3QOcyX_Fp9ZqD7q8QCma0fEyZym8SjkzXdAFX8M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP540177.RAxgZS3QOcyX_Fp9ZqD7q8QCma0fEyZym8SjkzXdAFX8M130_provenance.
- NP540177.RAxgZS3QOcyX_Fp9ZqD7q8QCma0fEyZym8SjkzXdAFX8M130_assertion description "[To report the identification of the T1174S SCN1A (NaV 1.1) mutation in a three-generation family with both epileptic and familial hemiplegic migraine (FHM) phenotypes and clarify the pathomechanism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP540177.RAxgZS3QOcyX_Fp9ZqD7q8QCma0fEyZym8SjkzXdAFX8M130_provenance.
- NP540177.RAxgZS3QOcyX_Fp9ZqD7q8QCma0fEyZym8SjkzXdAFX8M130_assertion evidence source_evidence_literature NP540177.RAxgZS3QOcyX_Fp9ZqD7q8QCma0fEyZym8SjkzXdAFX8M130_provenance.
- NP540177.RAxgZS3QOcyX_Fp9ZqD7q8QCma0fEyZym8SjkzXdAFX8M130_assertion SIO_000772 23398611 NP540177.RAxgZS3QOcyX_Fp9ZqD7q8QCma0fEyZym8SjkzXdAFX8M130_provenance.
- NP540177.RAxgZS3QOcyX_Fp9ZqD7q8QCma0fEyZym8SjkzXdAFX8M130_assertion wasDerivedFrom befree-20140225 NP540177.RAxgZS3QOcyX_Fp9ZqD7q8QCma0fEyZym8SjkzXdAFX8M130_provenance.
- NP540177.RAxgZS3QOcyX_Fp9ZqD7q8QCma0fEyZym8SjkzXdAFX8M130_assertion wasGeneratedBy ECO_0000203 NP540177.RAxgZS3QOcyX_Fp9ZqD7q8QCma0fEyZym8SjkzXdAFX8M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP540177.RAxgZS3QOcyX_Fp9ZqD7q8QCma0fEyZym8SjkzXdAFX8M130_provenance.