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- source_evidence_literature type ECO_0000212 NP669017.RAKGJowVnDHFzec-SmRa7AQW31AEluE14ZYaxtSJffHQI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP669017.RAKGJowVnDHFzec-SmRa7AQW31AEluE14ZYaxtSJffHQI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP669017.RAKGJowVnDHFzec-SmRa7AQW31AEluE14ZYaxtSJffHQI130_provenance.
- NP669017.RAKGJowVnDHFzec-SmRa7AQW31AEluE14ZYaxtSJffHQI130_assertion description "[Familial hemiplegic migraine (FHM) is genetically heterogeneous with mutations in the CACNA1A (FHM1), ATP1A2 (FHM2) and SCN1A (FHM3) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP669017.RAKGJowVnDHFzec-SmRa7AQW31AEluE14ZYaxtSJffHQI130_provenance.
- NP669017.RAKGJowVnDHFzec-SmRa7AQW31AEluE14ZYaxtSJffHQI130_assertion evidence source_evidence_literature NP669017.RAKGJowVnDHFzec-SmRa7AQW31AEluE14ZYaxtSJffHQI130_provenance.
- NP669017.RAKGJowVnDHFzec-SmRa7AQW31AEluE14ZYaxtSJffHQI130_assertion SIO_000772 18451712 NP669017.RAKGJowVnDHFzec-SmRa7AQW31AEluE14ZYaxtSJffHQI130_provenance.
- NP669017.RAKGJowVnDHFzec-SmRa7AQW31AEluE14ZYaxtSJffHQI130_assertion wasDerivedFrom befree-2016 NP669017.RAKGJowVnDHFzec-SmRa7AQW31AEluE14ZYaxtSJffHQI130_provenance.
- NP669017.RAKGJowVnDHFzec-SmRa7AQW31AEluE14ZYaxtSJffHQI130_assertion wasGeneratedBy ECO_0000203 NP669017.RAKGJowVnDHFzec-SmRa7AQW31AEluE14ZYaxtSJffHQI130_provenance.
- befree-2016 importedOn "2016-02-19" NP669017.RAKGJowVnDHFzec-SmRa7AQW31AEluE14ZYaxtSJffHQI130_provenance.