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- source_evidence_literature type ECO_0000212 NP506879.RAiDhFLmO3eFlB9QCLuBBIOYt1eP3a1_NJ_7vuEb5LKtU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP506879.RAiDhFLmO3eFlB9QCLuBBIOYt1eP3a1_NJ_7vuEb5LKtU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP506879.RAiDhFLmO3eFlB9QCLuBBIOYt1eP3a1_NJ_7vuEb5LKtU130_provenance.
- NP506879.RAiDhFLmO3eFlB9QCLuBBIOYt1eP3a1_NJ_7vuEb5LKtU130_assertion description "[These results suggest a molecular phenotype in which discrete sets of differentially expressed genes are associated with genetically determined susceptibility (Il1b, Tnf, and Stat6) or resistance (Il15 and Selp) to alveolar bone loss, providing insight into the genetic etiology of this complex disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP506879.RAiDhFLmO3eFlB9QCLuBBIOYt1eP3a1_NJ_7vuEb5LKtU130_provenance.
- NP506879.RAiDhFLmO3eFlB9QCLuBBIOYt1eP3a1_NJ_7vuEb5LKtU130_assertion evidence source_evidence_literature NP506879.RAiDhFLmO3eFlB9QCLuBBIOYt1eP3a1_NJ_7vuEb5LKtU130_provenance.
- NP506879.RAiDhFLmO3eFlB9QCLuBBIOYt1eP3a1_NJ_7vuEb5LKtU130_assertion SIO_000772 15271905 NP506879.RAiDhFLmO3eFlB9QCLuBBIOYt1eP3a1_NJ_7vuEb5LKtU130_provenance.
- NP506879.RAiDhFLmO3eFlB9QCLuBBIOYt1eP3a1_NJ_7vuEb5LKtU130_assertion wasDerivedFrom befree-20150227 NP506879.RAiDhFLmO3eFlB9QCLuBBIOYt1eP3a1_NJ_7vuEb5LKtU130_provenance.
- NP506879.RAiDhFLmO3eFlB9QCLuBBIOYt1eP3a1_NJ_7vuEb5LKtU130_assertion wasGeneratedBy ECO_0000203 NP506879.RAiDhFLmO3eFlB9QCLuBBIOYt1eP3a1_NJ_7vuEb5LKtU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP506879.RAiDhFLmO3eFlB9QCLuBBIOYt1eP3a1_NJ_7vuEb5LKtU130_provenance.