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- source_evidence_literature type ECO_0000212 NP492605.RAIj2HcpaZ-VoMYy6l_rStTRany2I-Khb17My2NRefP3k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP492605.RAIj2HcpaZ-VoMYy6l_rStTRany2I-Khb17My2NRefP3k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP492605.RAIj2HcpaZ-VoMYy6l_rStTRany2I-Khb17My2NRefP3k130_provenance.
- NP492605.RAIj2HcpaZ-VoMYy6l_rStTRany2I-Khb17My2NRefP3k130_assertion description "[Two WNK isoforms, WNK1 and WNK4, have been identified as the disease genes for a rare monogenic hypertension syndrome (Gordon's syndrome or pseudohypoaldosteronism type 2 [PHA2]) implicating them in salt homeostasis by the kidney.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492605.RAIj2HcpaZ-VoMYy6l_rStTRany2I-Khb17My2NRefP3k130_provenance.
- NP492605.RAIj2HcpaZ-VoMYy6l_rStTRany2I-Khb17My2NRefP3k130_assertion evidence source_evidence_literature NP492605.RAIj2HcpaZ-VoMYy6l_rStTRany2I-Khb17My2NRefP3k130_provenance.
- NP492605.RAIj2HcpaZ-VoMYy6l_rStTRany2I-Khb17My2NRefP3k130_assertion SIO_000772 15866321 NP492605.RAIj2HcpaZ-VoMYy6l_rStTRany2I-Khb17My2NRefP3k130_provenance.
- NP492605.RAIj2HcpaZ-VoMYy6l_rStTRany2I-Khb17My2NRefP3k130_assertion wasDerivedFrom befree-2016 NP492605.RAIj2HcpaZ-VoMYy6l_rStTRany2I-Khb17My2NRefP3k130_provenance.
- NP492605.RAIj2HcpaZ-VoMYy6l_rStTRany2I-Khb17My2NRefP3k130_assertion wasGeneratedBy ECO_0000203 NP492605.RAIj2HcpaZ-VoMYy6l_rStTRany2I-Khb17My2NRefP3k130_provenance.
- befree-2016 importedOn "2016-02-19" NP492605.RAIj2HcpaZ-VoMYy6l_rStTRany2I-Khb17My2NRefP3k130_provenance.