Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1244644.RAbDngRMa5c7gBRwVD7hD5wqjdbPoPq2ynWUzJ0nC0HWU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1244644.RAbDngRMa5c7gBRwVD7hD5wqjdbPoPq2ynWUzJ0nC0HWU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1244644.RAbDngRMa5c7gBRwVD7hD5wqjdbPoPq2ynWUzJ0nC0HWU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1244644.RAbDngRMa5c7gBRwVD7hD5wqjdbPoPq2ynWUzJ0nC0HWU130_provenance.
- NP1244644.RAbDngRMa5c7gBRwVD7hD5wqjdbPoPq2ynWUzJ0nC0HWU130_assertion description "[Taken together, our data suggest that rare deleterious CHD7 alleles contribute to the mutational burden of patients with both KS and normosmic forms of IGD in the absence of full CHARGE syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1244644.RAbDngRMa5c7gBRwVD7hD5wqjdbPoPq2ynWUzJ0nC0HWU130_provenance.
- NP1244644.RAbDngRMa5c7gBRwVD7hD5wqjdbPoPq2ynWUzJ0nC0HWU130_assertion evidence source_evidence_literature NP1244644.RAbDngRMa5c7gBRwVD7hD5wqjdbPoPq2ynWUzJ0nC0HWU130_provenance.
- NP1244644.RAbDngRMa5c7gBRwVD7hD5wqjdbPoPq2ynWUzJ0nC0HWU130_assertion SIO_000772 25472840 NP1244644.RAbDngRMa5c7gBRwVD7hD5wqjdbPoPq2ynWUzJ0nC0HWU130_provenance.
- NP1244644.RAbDngRMa5c7gBRwVD7hD5wqjdbPoPq2ynWUzJ0nC0HWU130_assertion wasDerivedFrom befree-2016 NP1244644.RAbDngRMa5c7gBRwVD7hD5wqjdbPoPq2ynWUzJ0nC0HWU130_provenance.
- NP1244644.RAbDngRMa5c7gBRwVD7hD5wqjdbPoPq2ynWUzJ0nC0HWU130_assertion wasGeneratedBy ECO_0000203 NP1244644.RAbDngRMa5c7gBRwVD7hD5wqjdbPoPq2ynWUzJ0nC0HWU130_provenance.
- befree-2016 importedOn "2016-02-19" NP1244644.RAbDngRMa5c7gBRwVD7hD5wqjdbPoPq2ynWUzJ0nC0HWU130_provenance.