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- source_evidence_literature type ECO_0000212 NP798176.RAgjt-wjAC5_iCL1wfdAVfNismE7DI5ebRliQOJcVIT5w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP798176.RAgjt-wjAC5_iCL1wfdAVfNismE7DI5ebRliQOJcVIT5w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP798176.RAgjt-wjAC5_iCL1wfdAVfNismE7DI5ebRliQOJcVIT5w130_provenance.
- NP798176.RAgjt-wjAC5_iCL1wfdAVfNismE7DI5ebRliQOJcVIT5w130_assertion description "[A genetic mutation within its MSP domain, P56S, was identified in familial forms of motor neuron diseases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP798176.RAgjt-wjAC5_iCL1wfdAVfNismE7DI5ebRliQOJcVIT5w130_provenance.
- NP798176.RAgjt-wjAC5_iCL1wfdAVfNismE7DI5ebRliQOJcVIT5w130_assertion evidence source_evidence_literature NP798176.RAgjt-wjAC5_iCL1wfdAVfNismE7DI5ebRliQOJcVIT5w130_provenance.
- NP798176.RAgjt-wjAC5_iCL1wfdAVfNismE7DI5ebRliQOJcVIT5w130_assertion SIO_000772 20207736 NP798176.RAgjt-wjAC5_iCL1wfdAVfNismE7DI5ebRliQOJcVIT5w130_provenance.
- NP798176.RAgjt-wjAC5_iCL1wfdAVfNismE7DI5ebRliQOJcVIT5w130_assertion wasDerivedFrom befree-2016 NP798176.RAgjt-wjAC5_iCL1wfdAVfNismE7DI5ebRliQOJcVIT5w130_provenance.
- NP798176.RAgjt-wjAC5_iCL1wfdAVfNismE7DI5ebRliQOJcVIT5w130_assertion wasGeneratedBy ECO_0000203 NP798176.RAgjt-wjAC5_iCL1wfdAVfNismE7DI5ebRliQOJcVIT5w130_provenance.
- befree-2016 importedOn "2016-02-19" NP798176.RAgjt-wjAC5_iCL1wfdAVfNismE7DI5ebRliQOJcVIT5w130_provenance.