Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1231932.RACXP4WwemCwLROayoUjaUUDDsb7xQg9bXuCXCxShmCkE130_assertion> ?p ?o ?g. }
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- NP1231932.RACXP4WwemCwLROayoUjaUUDDsb7xQg9bXuCXCxShmCkE130_assertion type Assertion NP1231932.RACXP4WwemCwLROayoUjaUUDDsb7xQg9bXuCXCxShmCkE130_head.
- NP1231932.RACXP4WwemCwLROayoUjaUUDDsb7xQg9bXuCXCxShmCkE130_assertion description "[The KCNT1:Arg1106Gln mutation was identified in a patient with syncope.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1231932.RACXP4WwemCwLROayoUjaUUDDsb7xQg9bXuCXCxShmCkE130_provenance.
- NP1231932.RACXP4WwemCwLROayoUjaUUDDsb7xQg9bXuCXCxShmCkE130_assertion evidence source_evidence_literature NP1231932.RACXP4WwemCwLROayoUjaUUDDsb7xQg9bXuCXCxShmCkE130_provenance.
- NP1231932.RACXP4WwemCwLROayoUjaUUDDsb7xQg9bXuCXCxShmCkE130_assertion SIO_000772 25339316 NP1231932.RACXP4WwemCwLROayoUjaUUDDsb7xQg9bXuCXCxShmCkE130_provenance.
- NP1231932.RACXP4WwemCwLROayoUjaUUDDsb7xQg9bXuCXCxShmCkE130_assertion wasDerivedFrom befree-2016 NP1231932.RACXP4WwemCwLROayoUjaUUDDsb7xQg9bXuCXCxShmCkE130_provenance.
- NP1231932.RACXP4WwemCwLROayoUjaUUDDsb7xQg9bXuCXCxShmCkE130_assertion wasGeneratedBy ECO_0000203 NP1231932.RACXP4WwemCwLROayoUjaUUDDsb7xQg9bXuCXCxShmCkE130_provenance.