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- source_evidence_literature type ECO_0000212 NP924732.RAc92d0PyN-z7_Jr6TBUk0RMKxd4L4xskqvT-AkngfqvU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP924732.RAc92d0PyN-z7_Jr6TBUk0RMKxd4L4xskqvT-AkngfqvU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP924732.RAc92d0PyN-z7_Jr6TBUk0RMKxd4L4xskqvT-AkngfqvU130_provenance.
- NP924732.RAc92d0PyN-z7_Jr6TBUk0RMKxd4L4xskqvT-AkngfqvU130_assertion wasGeneratedBy ECO_0000203 NP924732.RAc92d0PyN-z7_Jr6TBUk0RMKxd4L4xskqvT-AkngfqvU130_provenance.
- NP924732.RAc92d0PyN-z7_Jr6TBUk0RMKxd4L4xskqvT-AkngfqvU130_assertion wasDerivedFrom befree-20140225 NP924732.RAc92d0PyN-z7_Jr6TBUk0RMKxd4L4xskqvT-AkngfqvU130_provenance.
- NP924732.RAc92d0PyN-z7_Jr6TBUk0RMKxd4L4xskqvT-AkngfqvU130_assertion SIO_000772 9727001 NP924732.RAc92d0PyN-z7_Jr6TBUk0RMKxd4L4xskqvT-AkngfqvU130_provenance.
- NP924732.RAc92d0PyN-z7_Jr6TBUk0RMKxd4L4xskqvT-AkngfqvU130_assertion evidence source_evidence_literature NP924732.RAc92d0PyN-z7_Jr6TBUk0RMKxd4L4xskqvT-AkngfqvU130_provenance.
- NP924732.RAc92d0PyN-z7_Jr6TBUk0RMKxd4L4xskqvT-AkngfqvU130_assertion description "[Loss of function mutations in kidney Kir1.1 (renal outer medullary potassium channel, KCNJ1) inwardly rectifying potassium channels can be found in patients suffering from hyperprostaglandin E syndrome (HPS), the antenatal form of Bartter syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP924732.RAc92d0PyN-z7_Jr6TBUk0RMKxd4L4xskqvT-AkngfqvU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP924732.RAc92d0PyN-z7_Jr6TBUk0RMKxd4L4xskqvT-AkngfqvU130_provenance.