Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_assertion> ?p ?o ?g. }
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- NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_assertion type Assertion NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_head.
- NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_assertion description "[Although mutations in eight different genes (EDNRB, EDN3, ECE1, SOX10, RET, GDNF, NTN, SIP1) have been identified in affected individuals, it is now clear that RET and EDNRB are the primary genes implicated in the etiology of HSCR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_provenance.
- NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_assertion evidence source_evidence_literature NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_provenance.
- NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_assertion SIO_000772 16618617 NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_provenance.
- NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_assertion wasDerivedFrom befree-20140225 NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_provenance.
- NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_assertion wasGeneratedBy ECO_0000203 NP610279.RAnRza_9LwqGrwuwp3C10YTj9yXiKkHpEa_jRTx1yMKdc130_provenance.