Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP545150.RA7xT9z95XIpYHhljWPho89It1wIZ2OBsiL4l2vPnR-HI130_assertion> ?p ?o ?g. }
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- NP545150.RA7xT9z95XIpYHhljWPho89It1wIZ2OBsiL4l2vPnR-HI130_assertion type Assertion NP545150.RA7xT9z95XIpYHhljWPho89It1wIZ2OBsiL4l2vPnR-HI130_head.
- NP545150.RA7xT9z95XIpYHhljWPho89It1wIZ2OBsiL4l2vPnR-HI130_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." NP545150.RA7xT9z95XIpYHhljWPho89It1wIZ2OBsiL4l2vPnR-HI130_provenance.
- NP545150.RA7xT9z95XIpYHhljWPho89It1wIZ2OBsiL4l2vPnR-HI130_assertion evidence source_evidence_literature NP545150.RA7xT9z95XIpYHhljWPho89It1wIZ2OBsiL4l2vPnR-HI130_provenance.
- NP545150.RA7xT9z95XIpYHhljWPho89It1wIZ2OBsiL4l2vPnR-HI130_assertion SIO_000772 16618617 NP545150.RA7xT9z95XIpYHhljWPho89It1wIZ2OBsiL4l2vPnR-HI130_provenance.
- NP545150.RA7xT9z95XIpYHhljWPho89It1wIZ2OBsiL4l2vPnR-HI130_assertion wasDerivedFrom befree-2016 NP545150.RA7xT9z95XIpYHhljWPho89It1wIZ2OBsiL4l2vPnR-HI130_provenance.
- NP545150.RA7xT9z95XIpYHhljWPho89It1wIZ2OBsiL4l2vPnR-HI130_assertion wasGeneratedBy ECO_0000203 NP545150.RA7xT9z95XIpYHhljWPho89It1wIZ2OBsiL4l2vPnR-HI130_provenance.