Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP438348.RAtuoN17BRbapMupObCF3-imCnPkFIjM_1zddTrjhEdss130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP438348.RAtuoN17BRbapMupObCF3-imCnPkFIjM_1zddTrjhEdss130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP438348.RAtuoN17BRbapMupObCF3-imCnPkFIjM_1zddTrjhEdss130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP438348.RAtuoN17BRbapMupObCF3-imCnPkFIjM_1zddTrjhEdss130_provenance.
- NP438348.RAtuoN17BRbapMupObCF3-imCnPkFIjM_1zddTrjhEdss130_assertion description "[Connexin 26 and connexin 30 mutations in children with nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP438348.RAtuoN17BRbapMupObCF3-imCnPkFIjM_1zddTrjhEdss130_provenance.
- NP438348.RAtuoN17BRbapMupObCF3-imCnPkFIjM_1zddTrjhEdss130_assertion evidence source_evidence_literature NP438348.RAtuoN17BRbapMupObCF3-imCnPkFIjM_1zddTrjhEdss130_provenance.
- NP438348.RAtuoN17BRbapMupObCF3-imCnPkFIjM_1zddTrjhEdss130_assertion SIO_000772 15064611 NP438348.RAtuoN17BRbapMupObCF3-imCnPkFIjM_1zddTrjhEdss130_provenance.
- NP438348.RAtuoN17BRbapMupObCF3-imCnPkFIjM_1zddTrjhEdss130_assertion wasDerivedFrom befree-2016 NP438348.RAtuoN17BRbapMupObCF3-imCnPkFIjM_1zddTrjhEdss130_provenance.
- NP438348.RAtuoN17BRbapMupObCF3-imCnPkFIjM_1zddTrjhEdss130_assertion wasGeneratedBy ECO_0000203 NP438348.RAtuoN17BRbapMupObCF3-imCnPkFIjM_1zddTrjhEdss130_provenance.
- befree-2016 importedOn "2016-02-19" NP438348.RAtuoN17BRbapMupObCF3-imCnPkFIjM_1zddTrjhEdss130_provenance.