Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP772327.RAnFHWQziZ5OnW0UTa6zlTAPCUep10RKV-GQNkngp-2OY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP772327.RAnFHWQziZ5OnW0UTa6zlTAPCUep10RKV-GQNkngp-2OY130_assertion type Assertion NP772327.RAnFHWQziZ5OnW0UTa6zlTAPCUep10RKV-GQNkngp-2OY130_head.
- NP772327.RAnFHWQziZ5OnW0UTa6zlTAPCUep10RKV-GQNkngp-2OY130_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." NP772327.RAnFHWQziZ5OnW0UTa6zlTAPCUep10RKV-GQNkngp-2OY130_provenance.
- NP772327.RAnFHWQziZ5OnW0UTa6zlTAPCUep10RKV-GQNkngp-2OY130_assertion evidence source_evidence_literature NP772327.RAnFHWQziZ5OnW0UTa6zlTAPCUep10RKV-GQNkngp-2OY130_provenance.
- NP772327.RAnFHWQziZ5OnW0UTa6zlTAPCUep10RKV-GQNkngp-2OY130_assertion SIO_000772 16618617 NP772327.RAnFHWQziZ5OnW0UTa6zlTAPCUep10RKV-GQNkngp-2OY130_provenance.
- NP772327.RAnFHWQziZ5OnW0UTa6zlTAPCUep10RKV-GQNkngp-2OY130_assertion wasDerivedFrom befree-20140225 NP772327.RAnFHWQziZ5OnW0UTa6zlTAPCUep10RKV-GQNkngp-2OY130_provenance.
- NP772327.RAnFHWQziZ5OnW0UTa6zlTAPCUep10RKV-GQNkngp-2OY130_assertion wasGeneratedBy ECO_0000203 NP772327.RAnFHWQziZ5OnW0UTa6zlTAPCUep10RKV-GQNkngp-2OY130_provenance.