Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP654635.RA-OJIJ9DddIrDX5DFOys2s4Jam49l-liHObVQhKrfaGc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP654635.RA-OJIJ9DddIrDX5DFOys2s4Jam49l-liHObVQhKrfaGc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP654635.RA-OJIJ9DddIrDX5DFOys2s4Jam49l-liHObVQhKrfaGc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP654635.RA-OJIJ9DddIrDX5DFOys2s4Jam49l-liHObVQhKrfaGc130_provenance.
- NP654635.RA-OJIJ9DddIrDX5DFOys2s4Jam49l-liHObVQhKrfaGc130_assertion description "[Multiple mutations in the CLCN1 gene coding for the voltage-gated chloride channel have been documented to cause myotonia congenita.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP654635.RA-OJIJ9DddIrDX5DFOys2s4Jam49l-liHObVQhKrfaGc130_provenance.
- NP654635.RA-OJIJ9DddIrDX5DFOys2s4Jam49l-liHObVQhKrfaGc130_assertion evidence source_evidence_literature NP654635.RA-OJIJ9DddIrDX5DFOys2s4Jam49l-liHObVQhKrfaGc130_provenance.
- NP654635.RA-OJIJ9DddIrDX5DFOys2s4Jam49l-liHObVQhKrfaGc130_assertion SIO_000772 18263754 NP654635.RA-OJIJ9DddIrDX5DFOys2s4Jam49l-liHObVQhKrfaGc130_provenance.
- NP654635.RA-OJIJ9DddIrDX5DFOys2s4Jam49l-liHObVQhKrfaGc130_assertion wasDerivedFrom befree-2016 NP654635.RA-OJIJ9DddIrDX5DFOys2s4Jam49l-liHObVQhKrfaGc130_provenance.
- NP654635.RA-OJIJ9DddIrDX5DFOys2s4Jam49l-liHObVQhKrfaGc130_assertion wasGeneratedBy ECO_0000203 NP654635.RA-OJIJ9DddIrDX5DFOys2s4Jam49l-liHObVQhKrfaGc130_provenance.
- befree-2016 importedOn "2016-02-19" NP654635.RA-OJIJ9DddIrDX5DFOys2s4Jam49l-liHObVQhKrfaGc130_provenance.