Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP874429.RAFvmCX1hB0X7donhLvr_-FSU5kCS7-subesCkeK0IGdU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP874429.RAFvmCX1hB0X7donhLvr_-FSU5kCS7-subesCkeK0IGdU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP874429.RAFvmCX1hB0X7donhLvr_-FSU5kCS7-subesCkeK0IGdU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP874429.RAFvmCX1hB0X7donhLvr_-FSU5kCS7-subesCkeK0IGdU130_provenance.
- NP874429.RAFvmCX1hB0X7donhLvr_-FSU5kCS7-subesCkeK0IGdU130_assertion description "[However, it remains unknown how barttin interacts with CLC-K channels in mammalian cells and how the mutations of barttin lead to Bartter syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP874429.RAFvmCX1hB0X7donhLvr_-FSU5kCS7-subesCkeK0IGdU130_provenance.
- NP874429.RAFvmCX1hB0X7donhLvr_-FSU5kCS7-subesCkeK0IGdU130_assertion evidence source_evidence_literature NP874429.RAFvmCX1hB0X7donhLvr_-FSU5kCS7-subesCkeK0IGdU130_provenance.
- NP874429.RAFvmCX1hB0X7donhLvr_-FSU5kCS7-subesCkeK0IGdU130_assertion SIO_000772 12761627 NP874429.RAFvmCX1hB0X7donhLvr_-FSU5kCS7-subesCkeK0IGdU130_provenance.
- NP874429.RAFvmCX1hB0X7donhLvr_-FSU5kCS7-subesCkeK0IGdU130_assertion wasDerivedFrom befree-20150227 NP874429.RAFvmCX1hB0X7donhLvr_-FSU5kCS7-subesCkeK0IGdU130_provenance.
- NP874429.RAFvmCX1hB0X7donhLvr_-FSU5kCS7-subesCkeK0IGdU130_assertion wasGeneratedBy ECO_0000203 NP874429.RAFvmCX1hB0X7donhLvr_-FSU5kCS7-subesCkeK0IGdU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP874429.RAFvmCX1hB0X7donhLvr_-FSU5kCS7-subesCkeK0IGdU130_provenance.