Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP332861.RARelvUTY90uxtYOLxwVWhatI5uExawdGbT0MTqehrOtA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP332861.RARelvUTY90uxtYOLxwVWhatI5uExawdGbT0MTqehrOtA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP332861.RARelvUTY90uxtYOLxwVWhatI5uExawdGbT0MTqehrOtA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP332861.RARelvUTY90uxtYOLxwVWhatI5uExawdGbT0MTqehrOtA130_provenance.
- NP332861.RARelvUTY90uxtYOLxwVWhatI5uExawdGbT0MTqehrOtA130_assertion description "[Large-scale deletions and SMADIP1 truncating mutations in syndromic Hirschsprung disease with involvement of midline structures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP332861.RARelvUTY90uxtYOLxwVWhatI5uExawdGbT0MTqehrOtA130_provenance.
- NP332861.RARelvUTY90uxtYOLxwVWhatI5uExawdGbT0MTqehrOtA130_assertion evidence source_evidence_literature NP332861.RARelvUTY90uxtYOLxwVWhatI5uExawdGbT0MTqehrOtA130_provenance.
- NP332861.RARelvUTY90uxtYOLxwVWhatI5uExawdGbT0MTqehrOtA130_assertion SIO_000772 11595972 NP332861.RARelvUTY90uxtYOLxwVWhatI5uExawdGbT0MTqehrOtA130_provenance.
- NP332861.RARelvUTY90uxtYOLxwVWhatI5uExawdGbT0MTqehrOtA130_assertion wasDerivedFrom befree-2016 NP332861.RARelvUTY90uxtYOLxwVWhatI5uExawdGbT0MTqehrOtA130_provenance.
- NP332861.RARelvUTY90uxtYOLxwVWhatI5uExawdGbT0MTqehrOtA130_assertion wasGeneratedBy ECO_0000203 NP332861.RARelvUTY90uxtYOLxwVWhatI5uExawdGbT0MTqehrOtA130_provenance.
- befree-2016 importedOn "2016-02-19" NP332861.RARelvUTY90uxtYOLxwVWhatI5uExawdGbT0MTqehrOtA130_provenance.