Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_assertion> ?p ?o ?g. }
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- NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_assertion type Assertion NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_head.
- NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_assertion description "[Four subjects (aged 31-50 years) with co-occurring RET mutations in exons 10 (C609R; n=1) and 13 (Y791F, n=3) had sporadic short-segment HD with normal thyroid US and serum calcitonin.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_provenance.
- NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_assertion evidence source_evidence_literature NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_provenance.
- NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_assertion SIO_000772 23744765 NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_provenance.
- NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_assertion wasDerivedFrom befree-20140225 NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_provenance.
- NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_assertion wasGeneratedBy ECO_0000203 NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_provenance.