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- NP782531.RA-Vzb97dQpD4wVeLORCv5g7s1f2zNpjMTS9rx6dJDBqg130_assertion type Assertion NP782531.RA-Vzb97dQpD4wVeLORCv5g7s1f2zNpjMTS9rx6dJDBqg130_head.
- NP782531.RA-Vzb97dQpD4wVeLORCv5g7s1f2zNpjMTS9rx6dJDBqg130_assertion wasGeneratedBy ECO_0000203 NP782531.RA-Vzb97dQpD4wVeLORCv5g7s1f2zNpjMTS9rx6dJDBqg130_provenance.
- NP782531.RA-Vzb97dQpD4wVeLORCv5g7s1f2zNpjMTS9rx6dJDBqg130_assertion wasDerivedFrom befree-20150227 NP782531.RA-Vzb97dQpD4wVeLORCv5g7s1f2zNpjMTS9rx6dJDBqg130_provenance.
- NP782531.RA-Vzb97dQpD4wVeLORCv5g7s1f2zNpjMTS9rx6dJDBqg130_assertion SIO_000772 22407275 NP782531.RA-Vzb97dQpD4wVeLORCv5g7s1f2zNpjMTS9rx6dJDBqg130_provenance.
- NP782531.RA-Vzb97dQpD4wVeLORCv5g7s1f2zNpjMTS9rx6dJDBqg130_assertion evidence source_evidence_literature NP782531.RA-Vzb97dQpD4wVeLORCv5g7s1f2zNpjMTS9rx6dJDBqg130_provenance.
- NP782531.RA-Vzb97dQpD4wVeLORCv5g7s1f2zNpjMTS9rx6dJDBqg130_assertion description "[Myotonic dystrophy type 2 (DM2) is a common adult onset muscular dystrophy caused by a dominantly transmitted (CCTG)( n ) expansion in intron 1 of the CNBP gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP782531.RA-Vzb97dQpD4wVeLORCv5g7s1f2zNpjMTS9rx6dJDBqg130_provenance.