Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP816497.RAFxC0RSWz2aUyO-g3-Z5_QkY9abkR7BwVCOZWJWh9l-s130_assertion> ?p ?o ?g. }
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- NP816497.RAFxC0RSWz2aUyO-g3-Z5_QkY9abkR7BwVCOZWJWh9l-s130_assertion type Assertion NP816497.RAFxC0RSWz2aUyO-g3-Z5_QkY9abkR7BwVCOZWJWh9l-s130_head.
- NP816497.RAFxC0RSWz2aUyO-g3-Z5_QkY9abkR7BwVCOZWJWh9l-s130_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." NP816497.RAFxC0RSWz2aUyO-g3-Z5_QkY9abkR7BwVCOZWJWh9l-s130_provenance.
- NP816497.RAFxC0RSWz2aUyO-g3-Z5_QkY9abkR7BwVCOZWJWh9l-s130_assertion evidence source_evidence_literature NP816497.RAFxC0RSWz2aUyO-g3-Z5_QkY9abkR7BwVCOZWJWh9l-s130_provenance.
- NP816497.RAFxC0RSWz2aUyO-g3-Z5_QkY9abkR7BwVCOZWJWh9l-s130_assertion SIO_000772 16618617 NP816497.RAFxC0RSWz2aUyO-g3-Z5_QkY9abkR7BwVCOZWJWh9l-s130_provenance.
- NP816497.RAFxC0RSWz2aUyO-g3-Z5_QkY9abkR7BwVCOZWJWh9l-s130_assertion wasDerivedFrom befree-20150227 NP816497.RAFxC0RSWz2aUyO-g3-Z5_QkY9abkR7BwVCOZWJWh9l-s130_provenance.
- NP816497.RAFxC0RSWz2aUyO-g3-Z5_QkY9abkR7BwVCOZWJWh9l-s130_assertion wasGeneratedBy ECO_0000203 NP816497.RAFxC0RSWz2aUyO-g3-Z5_QkY9abkR7BwVCOZWJWh9l-s130_provenance.