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- source_evidence_literature type ECO_0000212 NP801477.RABR-acfk8nIA1WCp8jadY6aIVQy1R0f_RMgQPU8K43Uc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP801477.RABR-acfk8nIA1WCp8jadY6aIVQy1R0f_RMgQPU8K43Uc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP801477.RABR-acfk8nIA1WCp8jadY6aIVQy1R0f_RMgQPU8K43Uc130_provenance.
- NP801477.RABR-acfk8nIA1WCp8jadY6aIVQy1R0f_RMgQPU8K43Uc130_assertion wasGeneratedBy ECO_0000203 NP801477.RABR-acfk8nIA1WCp8jadY6aIVQy1R0f_RMgQPU8K43Uc130_provenance.
- NP801477.RABR-acfk8nIA1WCp8jadY6aIVQy1R0f_RMgQPU8K43Uc130_assertion wasDerivedFrom befree-20140225 NP801477.RABR-acfk8nIA1WCp8jadY6aIVQy1R0f_RMgQPU8K43Uc130_provenance.
- NP801477.RABR-acfk8nIA1WCp8jadY6aIVQy1R0f_RMgQPU8K43Uc130_assertion SIO_000772 18162506 NP801477.RABR-acfk8nIA1WCp8jadY6aIVQy1R0f_RMgQPU8K43Uc130_provenance.
- NP801477.RABR-acfk8nIA1WCp8jadY6aIVQy1R0f_RMgQPU8K43Uc130_assertion evidence source_evidence_literature NP801477.RABR-acfk8nIA1WCp8jadY6aIVQy1R0f_RMgQPU8K43Uc130_provenance.
- NP801477.RABR-acfk8nIA1WCp8jadY6aIVQy1R0f_RMgQPU8K43Uc130_assertion description "[We conclude that INS mutations are the second most common cause of PND and a rare cause of MODY.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP801477.RABR-acfk8nIA1WCp8jadY6aIVQy1R0f_RMgQPU8K43Uc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP801477.RABR-acfk8nIA1WCp8jadY6aIVQy1R0f_RMgQPU8K43Uc130_provenance.