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- source_evidence_literature type ECO_0000212 NP344931.RA1vHQXZIOZGQvZsM76B_D_jVTHdAys6k5L_Hmdv2tfFA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP344931.RA1vHQXZIOZGQvZsM76B_D_jVTHdAys6k5L_Hmdv2tfFA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP344931.RA1vHQXZIOZGQvZsM76B_D_jVTHdAys6k5L_Hmdv2tfFA130_provenance.
- NP344931.RA1vHQXZIOZGQvZsM76B_D_jVTHdAys6k5L_Hmdv2tfFA130_assertion description "[All four familial cases of BWS showed reduced methylation of KCNQ1OT1, suggesting that in these cases the imprinting switch mechanism is disturbed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP344931.RA1vHQXZIOZGQvZsM76B_D_jVTHdAys6k5L_Hmdv2tfFA130_provenance.
- NP344931.RA1vHQXZIOZGQvZsM76B_D_jVTHdAys6k5L_Hmdv2tfFA130_assertion evidence source_evidence_literature NP344931.RA1vHQXZIOZGQvZsM76B_D_jVTHdAys6k5L_Hmdv2tfFA130_provenance.
- NP344931.RA1vHQXZIOZGQvZsM76B_D_jVTHdAys6k5L_Hmdv2tfFA130_assertion SIO_000772 11181570 NP344931.RA1vHQXZIOZGQvZsM76B_D_jVTHdAys6k5L_Hmdv2tfFA130_provenance.
- NP344931.RA1vHQXZIOZGQvZsM76B_D_jVTHdAys6k5L_Hmdv2tfFA130_assertion wasDerivedFrom befree-20140225 NP344931.RA1vHQXZIOZGQvZsM76B_D_jVTHdAys6k5L_Hmdv2tfFA130_provenance.
- NP344931.RA1vHQXZIOZGQvZsM76B_D_jVTHdAys6k5L_Hmdv2tfFA130_assertion wasGeneratedBy ECO_0000203 NP344931.RA1vHQXZIOZGQvZsM76B_D_jVTHdAys6k5L_Hmdv2tfFA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP344931.RA1vHQXZIOZGQvZsM76B_D_jVTHdAys6k5L_Hmdv2tfFA130_provenance.