Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP686849.RAaXMpD0QdHk8X39al89A3kYboY6IuPAEumQF8QapupVM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP686849.RAaXMpD0QdHk8X39al89A3kYboY6IuPAEumQF8QapupVM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP686849.RAaXMpD0QdHk8X39al89A3kYboY6IuPAEumQF8QapupVM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP686849.RAaXMpD0QdHk8X39al89A3kYboY6IuPAEumQF8QapupVM130_provenance.
- NP686849.RAaXMpD0QdHk8X39al89A3kYboY6IuPAEumQF8QapupVM130_assertion description "[In accord, loss of function mutations in ENaC (PHA1) cause hypotension, whereas gain of function mutations (Liddle syndrome) result in hypertension.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP686849.RAaXMpD0QdHk8X39al89A3kYboY6IuPAEumQF8QapupVM130_provenance.
- NP686849.RAaXMpD0QdHk8X39al89A3kYboY6IuPAEumQF8QapupVM130_assertion evidence source_evidence_literature NP686849.RAaXMpD0QdHk8X39al89A3kYboY6IuPAEumQF8QapupVM130_provenance.
- NP686849.RAaXMpD0QdHk8X39al89A3kYboY6IuPAEumQF8QapupVM130_assertion SIO_000772 18691017 NP686849.RAaXMpD0QdHk8X39al89A3kYboY6IuPAEumQF8QapupVM130_provenance.
- NP686849.RAaXMpD0QdHk8X39al89A3kYboY6IuPAEumQF8QapupVM130_assertion wasDerivedFrom befree-2016 NP686849.RAaXMpD0QdHk8X39al89A3kYboY6IuPAEumQF8QapupVM130_provenance.
- NP686849.RAaXMpD0QdHk8X39al89A3kYboY6IuPAEumQF8QapupVM130_assertion wasGeneratedBy ECO_0000203 NP686849.RAaXMpD0QdHk8X39al89A3kYboY6IuPAEumQF8QapupVM130_provenance.
- befree-2016 importedOn "2016-02-19" NP686849.RAaXMpD0QdHk8X39al89A3kYboY6IuPAEumQF8QapupVM130_provenance.