Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1371037.RAlMXYsSRMccw_CabrThh5BUYOOeQ5Qg2eGrq3ItyanEk130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1371037.RAlMXYsSRMccw_CabrThh5BUYOOeQ5Qg2eGrq3ItyanEk130_assertion type Assertion NP1371037.RAlMXYsSRMccw_CabrThh5BUYOOeQ5Qg2eGrq3ItyanEk130_head.
- NP1371037.RAlMXYsSRMccw_CabrThh5BUYOOeQ5Qg2eGrq3ItyanEk130_assertion description "[Mutation of RET codon 768 is associated with the FMTC phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1371037.RAlMXYsSRMccw_CabrThh5BUYOOeQ5Qg2eGrq3ItyanEk130_provenance.
- NP1371037.RAlMXYsSRMccw_CabrThh5BUYOOeQ5Qg2eGrq3ItyanEk130_assertion evidence source_evidence_literature NP1371037.RAlMXYsSRMccw_CabrThh5BUYOOeQ5Qg2eGrq3ItyanEk130_provenance.
- NP1371037.RAlMXYsSRMccw_CabrThh5BUYOOeQ5Qg2eGrq3ItyanEk130_assertion SIO_000772 9111992 NP1371037.RAlMXYsSRMccw_CabrThh5BUYOOeQ5Qg2eGrq3ItyanEk130_provenance.
- NP1371037.RAlMXYsSRMccw_CabrThh5BUYOOeQ5Qg2eGrq3ItyanEk130_assertion wasDerivedFrom befree-2016 NP1371037.RAlMXYsSRMccw_CabrThh5BUYOOeQ5Qg2eGrq3ItyanEk130_provenance.
- NP1371037.RAlMXYsSRMccw_CabrThh5BUYOOeQ5Qg2eGrq3ItyanEk130_assertion wasGeneratedBy ECO_0000203 NP1371037.RAlMXYsSRMccw_CabrThh5BUYOOeQ5Qg2eGrq3ItyanEk130_provenance.