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- source_evidence_literature type ECO_0000212 NP754763.RAa10r3K445LunnGb373gMX4NqCSJCwW8vXMXk-am-Rw4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP754763.RAa10r3K445LunnGb373gMX4NqCSJCwW8vXMXk-am-Rw4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP754763.RAa10r3K445LunnGb373gMX4NqCSJCwW8vXMXk-am-Rw4130_provenance.
- NP754763.RAa10r3K445LunnGb373gMX4NqCSJCwW8vXMXk-am-Rw4130_assertion description "[The functional consequences of p.I12T differ from BSND mutations that cause renal failure and deafness in Bartter syndrome type IV.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP754763.RAa10r3K445LunnGb373gMX4NqCSJCwW8vXMXk-am-Rw4130_provenance.
- NP754763.RAa10r3K445LunnGb373gMX4NqCSJCwW8vXMXk-am-Rw4130_assertion evidence source_evidence_literature NP754763.RAa10r3K445LunnGb373gMX4NqCSJCwW8vXMXk-am-Rw4130_provenance.
- NP754763.RAa10r3K445LunnGb373gMX4NqCSJCwW8vXMXk-am-Rw4130_assertion SIO_000772 19646679 NP754763.RAa10r3K445LunnGb373gMX4NqCSJCwW8vXMXk-am-Rw4130_provenance.
- NP754763.RAa10r3K445LunnGb373gMX4NqCSJCwW8vXMXk-am-Rw4130_assertion wasDerivedFrom befree-2016 NP754763.RAa10r3K445LunnGb373gMX4NqCSJCwW8vXMXk-am-Rw4130_provenance.
- NP754763.RAa10r3K445LunnGb373gMX4NqCSJCwW8vXMXk-am-Rw4130_assertion wasGeneratedBy ECO_0000203 NP754763.RAa10r3K445LunnGb373gMX4NqCSJCwW8vXMXk-am-Rw4130_provenance.
- befree-2016 importedOn "2016-02-19" NP754763.RAa10r3K445LunnGb373gMX4NqCSJCwW8vXMXk-am-Rw4130_provenance.