Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_provenance.
- NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_assertion description "[This study was conducted to report a family affected by benign hereditary chorea in which a large deletion including TTF1, PAX9, and other genes was identified and results in oligodontia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_provenance.
- NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_assertion evidence source_evidence_literature NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_provenance.
- NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_assertion SIO_000772 18445003 NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_provenance.
- NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_assertion wasDerivedFrom befree-2016 NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_provenance.
- NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_assertion wasGeneratedBy ECO_0000203 NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_provenance.
- befree-2016 importedOn "2016-02-19" NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_provenance.