Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP651932.RA-VYlbqTqMX2Xp75MgN9jP33yPbIJbE8X-rqnb55DfNk130_provenance.