Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_assertion> ?p ?o ?g. }
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- NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_assertion type Assertion NP668449.RAQUP7M2IyLFFw0f7LgdEhCTXVBECmfa3tf4V6133_hcc130_head.
- 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.