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- source_evidence_literature type ECO_0000212 NP963965.RAVUTgSg3o78PhO3_zjXNmv9PjLVLnnFfsU3dm5-bc_ww130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP963965.RAVUTgSg3o78PhO3_zjXNmv9PjLVLnnFfsU3dm5-bc_ww130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP963965.RAVUTgSg3o78PhO3_zjXNmv9PjLVLnnFfsU3dm5-bc_ww130_provenance.
- NP963965.RAVUTgSg3o78PhO3_zjXNmv9PjLVLnnFfsU3dm5-bc_ww130_assertion description "[Here we report the identification of mutations in STX1B, encoding syntaxin-1B, that are associated with both febrile seizures and epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963965.RAVUTgSg3o78PhO3_zjXNmv9PjLVLnnFfsU3dm5-bc_ww130_provenance.
- NP963965.RAVUTgSg3o78PhO3_zjXNmv9PjLVLnnFfsU3dm5-bc_ww130_assertion evidence source_evidence_literature NP963965.RAVUTgSg3o78PhO3_zjXNmv9PjLVLnnFfsU3dm5-bc_ww130_provenance.
- NP963965.RAVUTgSg3o78PhO3_zjXNmv9PjLVLnnFfsU3dm5-bc_ww130_assertion SIO_000772 25362483 NP963965.RAVUTgSg3o78PhO3_zjXNmv9PjLVLnnFfsU3dm5-bc_ww130_provenance.
- NP963965.RAVUTgSg3o78PhO3_zjXNmv9PjLVLnnFfsU3dm5-bc_ww130_assertion wasDerivedFrom befree-20150227 NP963965.RAVUTgSg3o78PhO3_zjXNmv9PjLVLnnFfsU3dm5-bc_ww130_provenance.
- NP963965.RAVUTgSg3o78PhO3_zjXNmv9PjLVLnnFfsU3dm5-bc_ww130_assertion wasGeneratedBy ECO_0000203 NP963965.RAVUTgSg3o78PhO3_zjXNmv9PjLVLnnFfsU3dm5-bc_ww130_provenance.
- befree-20150227 importedOn "2015-02-27" NP963965.RAVUTgSg3o78PhO3_zjXNmv9PjLVLnnFfsU3dm5-bc_ww130_provenance.