Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP438347.RAAeYK9-1-btbwYXFVtWcS4Bf6Trfc_hRLjBL5QDXAQA8130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP438347.RAAeYK9-1-btbwYXFVtWcS4Bf6Trfc_hRLjBL5QDXAQA8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP438347.RAAeYK9-1-btbwYXFVtWcS4Bf6Trfc_hRLjBL5QDXAQA8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP438347.RAAeYK9-1-btbwYXFVtWcS4Bf6Trfc_hRLjBL5QDXAQA8130_provenance.
- NP438347.RAAeYK9-1-btbwYXFVtWcS4Bf6Trfc_hRLjBL5QDXAQA8130_assertion description "[Children also underwent audiological testing to determine whether any correlation exists between Cx26 mutations and severity of hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP438347.RAAeYK9-1-btbwYXFVtWcS4Bf6Trfc_hRLjBL5QDXAQA8130_provenance.
- NP438347.RAAeYK9-1-btbwYXFVtWcS4Bf6Trfc_hRLjBL5QDXAQA8130_assertion evidence source_evidence_literature NP438347.RAAeYK9-1-btbwYXFVtWcS4Bf6Trfc_hRLjBL5QDXAQA8130_provenance.
- NP438347.RAAeYK9-1-btbwYXFVtWcS4Bf6Trfc_hRLjBL5QDXAQA8130_assertion SIO_000772 15064611 NP438347.RAAeYK9-1-btbwYXFVtWcS4Bf6Trfc_hRLjBL5QDXAQA8130_provenance.
- NP438347.RAAeYK9-1-btbwYXFVtWcS4Bf6Trfc_hRLjBL5QDXAQA8130_assertion wasDerivedFrom befree-2016 NP438347.RAAeYK9-1-btbwYXFVtWcS4Bf6Trfc_hRLjBL5QDXAQA8130_provenance.
- NP438347.RAAeYK9-1-btbwYXFVtWcS4Bf6Trfc_hRLjBL5QDXAQA8130_assertion wasGeneratedBy ECO_0000203 NP438347.RAAeYK9-1-btbwYXFVtWcS4Bf6Trfc_hRLjBL5QDXAQA8130_provenance.
- befree-2016 importedOn "2016-02-19" NP438347.RAAeYK9-1-btbwYXFVtWcS4Bf6Trfc_hRLjBL5QDXAQA8130_provenance.