Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_assertion> ?p ?o ?g. }
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- NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_assertion type Assertion NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_head.
- NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_assertion description "[Initially a codon 634 (exon 11) mutation was found in approximately 85% of patients with MEN 2A, and germline mutations in FMTC kindreds were more equally distributed throughout the RET proto-onocogene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_provenance.
- NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_assertion evidence source_evidence_literature NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_provenance.
- NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_assertion SIO_000772 17605401 NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_provenance.
- NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_assertion wasDerivedFrom befree-2016 NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_provenance.
- NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_assertion wasGeneratedBy ECO_0000203 NP618073.RAr-L6ZKi0VElMkOot0F8_YmoTDORIvF6HyUZ_qwrVoKE130_provenance.