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- source_evidence_literature type ECO_0000212 NP223110.RADTLlZOWPmGmZ6eOKVxcMQwod_O53H_RBB20jWxtp-5E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP223110.RADTLlZOWPmGmZ6eOKVxcMQwod_O53H_RBB20jWxtp-5E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP223110.RADTLlZOWPmGmZ6eOKVxcMQwod_O53H_RBB20jWxtp-5E130_provenance.
- NP223110.RADTLlZOWPmGmZ6eOKVxcMQwod_O53H_RBB20jWxtp-5E130_assertion description "[Human-mouse somatic cell hybrids, in which the human parental cells were fibroblastss from an individual with ADA-deficient SCID, also required human chromosomes 2 and 6 to express the ADA-complexing protein, indicating that neither ADCP-1 nor ADCP-2 is involved in the ADA deficiency in SCID.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP223110.RADTLlZOWPmGmZ6eOKVxcMQwod_O53H_RBB20jWxtp-5E130_provenance.
- NP223110.RADTLlZOWPmGmZ6eOKVxcMQwod_O53H_RBB20jWxtp-5E130_assertion evidence source_evidence_literature NP223110.RADTLlZOWPmGmZ6eOKVxcMQwod_O53H_RBB20jWxtp-5E130_provenance.
- NP223110.RADTLlZOWPmGmZ6eOKVxcMQwod_O53H_RBB20jWxtp-5E130_assertion SIO_000772 6933468 NP223110.RADTLlZOWPmGmZ6eOKVxcMQwod_O53H_RBB20jWxtp-5E130_provenance.
- NP223110.RADTLlZOWPmGmZ6eOKVxcMQwod_O53H_RBB20jWxtp-5E130_assertion wasDerivedFrom befree-20150227 NP223110.RADTLlZOWPmGmZ6eOKVxcMQwod_O53H_RBB20jWxtp-5E130_provenance.
- NP223110.RADTLlZOWPmGmZ6eOKVxcMQwod_O53H_RBB20jWxtp-5E130_assertion wasGeneratedBy ECO_0000203 NP223110.RADTLlZOWPmGmZ6eOKVxcMQwod_O53H_RBB20jWxtp-5E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP223110.RADTLlZOWPmGmZ6eOKVxcMQwod_O53H_RBB20jWxtp-5E130_provenance.