Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP477815.RADhmfkVxG1YT8oDsepAgM4LY710aCtsI5xBZ6DNxSUxQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP477815.RADhmfkVxG1YT8oDsepAgM4LY710aCtsI5xBZ6DNxSUxQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477815.RADhmfkVxG1YT8oDsepAgM4LY710aCtsI5xBZ6DNxSUxQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477815.RADhmfkVxG1YT8oDsepAgM4LY710aCtsI5xBZ6DNxSUxQ130_provenance.
- NP477815.RADhmfkVxG1YT8oDsepAgM4LY710aCtsI5xBZ6DNxSUxQ130_assertion description "[Mutations in connexin 31 (GJB3) and connexin 30.3 (GJB4), implicated in previous reports of EKV, and connexin 26 (GJB2), implicated in palmoplantar keratoderma, were unlikely given the lack of shared homozygous haplotypes in the regions surrounding these genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477815.RADhmfkVxG1YT8oDsepAgM4LY710aCtsI5xBZ6DNxSUxQ130_provenance.
- NP477815.RADhmfkVxG1YT8oDsepAgM4LY710aCtsI5xBZ6DNxSUxQ130_assertion evidence source_evidence_literature NP477815.RADhmfkVxG1YT8oDsepAgM4LY710aCtsI5xBZ6DNxSUxQ130_provenance.
- NP477815.RADhmfkVxG1YT8oDsepAgM4LY710aCtsI5xBZ6DNxSUxQ130_assertion SIO_000772 15668823 NP477815.RADhmfkVxG1YT8oDsepAgM4LY710aCtsI5xBZ6DNxSUxQ130_provenance.
- NP477815.RADhmfkVxG1YT8oDsepAgM4LY710aCtsI5xBZ6DNxSUxQ130_assertion wasDerivedFrom befree-2016 NP477815.RADhmfkVxG1YT8oDsepAgM4LY710aCtsI5xBZ6DNxSUxQ130_provenance.
- NP477815.RADhmfkVxG1YT8oDsepAgM4LY710aCtsI5xBZ6DNxSUxQ130_assertion wasGeneratedBy ECO_0000203 NP477815.RADhmfkVxG1YT8oDsepAgM4LY710aCtsI5xBZ6DNxSUxQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP477815.RADhmfkVxG1YT8oDsepAgM4LY710aCtsI5xBZ6DNxSUxQ130_provenance.