Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP481492.RADfQOCU9i_I86FHG81_h8oG6jj4VM9OWjQPT5iTqh6Po130_assertion> ?p ?o ?g. }
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- NP481492.RADfQOCU9i_I86FHG81_h8oG6jj4VM9OWjQPT5iTqh6Po130_assertion type Assertion NP481492.RADfQOCU9i_I86FHG81_h8oG6jj4VM9OWjQPT5iTqh6Po130_head.
- NP481492.RADfQOCU9i_I86FHG81_h8oG6jj4VM9OWjQPT5iTqh6Po130_assertion wasGeneratedBy ECO_0000203 NP481492.RADfQOCU9i_I86FHG81_h8oG6jj4VM9OWjQPT5iTqh6Po130_provenance.
- NP481492.RADfQOCU9i_I86FHG81_h8oG6jj4VM9OWjQPT5iTqh6Po130_assertion wasDerivedFrom befree-20140225 NP481492.RADfQOCU9i_I86FHG81_h8oG6jj4VM9OWjQPT5iTqh6Po130_provenance.
- NP481492.RADfQOCU9i_I86FHG81_h8oG6jj4VM9OWjQPT5iTqh6Po130_assertion SIO_000772 12734540 NP481492.RADfQOCU9i_I86FHG81_h8oG6jj4VM9OWjQPT5iTqh6Po130_provenance.
- NP481492.RADfQOCU9i_I86FHG81_h8oG6jj4VM9OWjQPT5iTqh6Po130_assertion evidence source_evidence_literature NP481492.RADfQOCU9i_I86FHG81_h8oG6jj4VM9OWjQPT5iTqh6Po130_provenance.
- NP481492.RADfQOCU9i_I86FHG81_h8oG6jj4VM9OWjQPT5iTqh6Po130_assertion description "[Germline mutations in the RET proto-oncogene are responsible for the development of human hereditary diseases, including multiple endocrine neoplasia (MEN) type 2A and 2B, familial medullary thyroid carcinoma (FMTC), and Hirschsprung's disease (HSCR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP481492.RADfQOCU9i_I86FHG81_h8oG6jj4VM9OWjQPT5iTqh6Po130_provenance.