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- source_evidence_literature type ECO_0000212 NP1013707.RAad4p_5x8p_9A-_z0LwX-I2ct9C7-UwiyqdMIrCdH4Bg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1013707.RAad4p_5x8p_9A-_z0LwX-I2ct9C7-UwiyqdMIrCdH4Bg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1013707.RAad4p_5x8p_9A-_z0LwX-I2ct9C7-UwiyqdMIrCdH4Bg130_provenance.
- NP1013707.RAad4p_5x8p_9A-_z0LwX-I2ct9C7-UwiyqdMIrCdH4Bg130_assertion description "[Besides identifying 8 SCN5A mutations in the present cohort, a KCNE3 T4A mutation was found in a 55-year-old male patient who had experienced several episodes of syncope.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1013707.RAad4p_5x8p_9A-_z0LwX-I2ct9C7-UwiyqdMIrCdH4Bg130_provenance.
- NP1013707.RAad4p_5x8p_9A-_z0LwX-I2ct9C7-UwiyqdMIrCdH4Bg130_assertion evidence source_evidence_literature NP1013707.RAad4p_5x8p_9A-_z0LwX-I2ct9C7-UwiyqdMIrCdH4Bg130_provenance.
- NP1013707.RAad4p_5x8p_9A-_z0LwX-I2ct9C7-UwiyqdMIrCdH4Bg130_assertion SIO_000772 22987075 NP1013707.RAad4p_5x8p_9A-_z0LwX-I2ct9C7-UwiyqdMIrCdH4Bg130_provenance.
- NP1013707.RAad4p_5x8p_9A-_z0LwX-I2ct9C7-UwiyqdMIrCdH4Bg130_assertion wasDerivedFrom befree-2016 NP1013707.RAad4p_5x8p_9A-_z0LwX-I2ct9C7-UwiyqdMIrCdH4Bg130_provenance.
- NP1013707.RAad4p_5x8p_9A-_z0LwX-I2ct9C7-UwiyqdMIrCdH4Bg130_assertion wasGeneratedBy ECO_0000203 NP1013707.RAad4p_5x8p_9A-_z0LwX-I2ct9C7-UwiyqdMIrCdH4Bg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1013707.RAad4p_5x8p_9A-_z0LwX-I2ct9C7-UwiyqdMIrCdH4Bg130_provenance.