Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1265943.RAjBHjWcgi4lQHPJI4nGeHR4Kzs1gJFruFXkjBdU5CPxk130_assertion> ?p ?o ?g. }
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- NP1265943.RAjBHjWcgi4lQHPJI4nGeHR4Kzs1gJFruFXkjBdU5CPxk130_assertion type Assertion NP1265943.RAjBHjWcgi4lQHPJI4nGeHR4Kzs1gJFruFXkjBdU5CPxk130_head.
- NP1265943.RAjBHjWcgi4lQHPJI4nGeHR4Kzs1gJFruFXkjBdU5CPxk130_assertion description "[In a small group of patients the identification of a constitutional deletion on the long arm of chromosome 13 indicated the location of the critical gene in region 13q14 Close linkage between the hereditary, non-deletion form of RB and the esterase-D gene, which is also located in 13q14, demonstrated that all hereditary forms of RB are due to defects in a gene at this locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1265943.RAjBHjWcgi4lQHPJI4nGeHR4Kzs1gJFruFXkjBdU5CPxk130_provenance.
- NP1265943.RAjBHjWcgi4lQHPJI4nGeHR4Kzs1gJFruFXkjBdU5CPxk130_assertion evidence source_evidence_literature NP1265943.RAjBHjWcgi4lQHPJI4nGeHR4Kzs1gJFruFXkjBdU5CPxk130_provenance.
- NP1265943.RAjBHjWcgi4lQHPJI4nGeHR4Kzs1gJFruFXkjBdU5CPxk130_assertion SIO_000772 2571113 NP1265943.RAjBHjWcgi4lQHPJI4nGeHR4Kzs1gJFruFXkjBdU5CPxk130_provenance.
- NP1265943.RAjBHjWcgi4lQHPJI4nGeHR4Kzs1gJFruFXkjBdU5CPxk130_assertion wasDerivedFrom befree-2016 NP1265943.RAjBHjWcgi4lQHPJI4nGeHR4Kzs1gJFruFXkjBdU5CPxk130_provenance.
- NP1265943.RAjBHjWcgi4lQHPJI4nGeHR4Kzs1gJFruFXkjBdU5CPxk130_assertion wasGeneratedBy ECO_0000203 NP1265943.RAjBHjWcgi4lQHPJI4nGeHR4Kzs1gJFruFXkjBdU5CPxk130_provenance.