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- source_evidence_literature type ECO_0000212 NP713210.RAKg_yl0Uf2LkPr2p0EDat9piNueqpQoto4Ox210h8ENw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP713210.RAKg_yl0Uf2LkPr2p0EDat9piNueqpQoto4Ox210h8ENw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP713210.RAKg_yl0Uf2LkPr2p0EDat9piNueqpQoto4Ox210h8ENw130_provenance.
- NP713210.RAKg_yl0Uf2LkPr2p0EDat9piNueqpQoto4Ox210h8ENw130_assertion description "[Brain dysfunction is the most important sequelae of the fragile X (FMR-1) mutation, the most common heritable cause of developmental disability.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713210.RAKg_yl0Uf2LkPr2p0EDat9piNueqpQoto4Ox210h8ENw130_provenance.
- NP713210.RAKg_yl0Uf2LkPr2p0EDat9piNueqpQoto4Ox210h8ENw130_assertion evidence source_evidence_literature NP713210.RAKg_yl0Uf2LkPr2p0EDat9piNueqpQoto4Ox210h8ENw130_provenance.
- NP713210.RAKg_yl0Uf2LkPr2p0EDat9piNueqpQoto4Ox210h8ENw130_assertion SIO_000772 7585014 NP713210.RAKg_yl0Uf2LkPr2p0EDat9piNueqpQoto4Ox210h8ENw130_provenance.
- NP713210.RAKg_yl0Uf2LkPr2p0EDat9piNueqpQoto4Ox210h8ENw130_assertion wasDerivedFrom befree-20140225 NP713210.RAKg_yl0Uf2LkPr2p0EDat9piNueqpQoto4Ox210h8ENw130_provenance.
- NP713210.RAKg_yl0Uf2LkPr2p0EDat9piNueqpQoto4Ox210h8ENw130_assertion wasGeneratedBy ECO_0000203 NP713210.RAKg_yl0Uf2LkPr2p0EDat9piNueqpQoto4Ox210h8ENw130_provenance.
- befree-20140225 importedOn "2014-02-25" NP713210.RAKg_yl0Uf2LkPr2p0EDat9piNueqpQoto4Ox210h8ENw130_provenance.