Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1260496.RAykUk60OL5Iy0e097zrfzyhdSFP_jmV4kOcPcxx2Zm7M130_assertion> ?p ?o ?g. }
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- NP1260496.RAykUk60OL5Iy0e097zrfzyhdSFP_jmV4kOcPcxx2Zm7M130_assertion type Assertion NP1260496.RAykUk60OL5Iy0e097zrfzyhdSFP_jmV4kOcPcxx2Zm7M130_head.
- NP1260496.RAykUk60OL5Iy0e097zrfzyhdSFP_jmV4kOcPcxx2Zm7M130_assertion wasGeneratedBy ECO_0000203 NP1260496.RAykUk60OL5Iy0e097zrfzyhdSFP_jmV4kOcPcxx2Zm7M130_provenance.
- NP1260496.RAykUk60OL5Iy0e097zrfzyhdSFP_jmV4kOcPcxx2Zm7M130_assertion wasDerivedFrom befree-2016 NP1260496.RAykUk60OL5Iy0e097zrfzyhdSFP_jmV4kOcPcxx2Zm7M130_provenance.
- NP1260496.RAykUk60OL5Iy0e097zrfzyhdSFP_jmV4kOcPcxx2Zm7M130_assertion SIO_000772 25645993 NP1260496.RAykUk60OL5Iy0e097zrfzyhdSFP_jmV4kOcPcxx2Zm7M130_provenance.
- NP1260496.RAykUk60OL5Iy0e097zrfzyhdSFP_jmV4kOcPcxx2Zm7M130_assertion evidence source_evidence_literature NP1260496.RAykUk60OL5Iy0e097zrfzyhdSFP_jmV4kOcPcxx2Zm7M130_provenance.
- NP1260496.RAykUk60OL5Iy0e097zrfzyhdSFP_jmV4kOcPcxx2Zm7M130_assertion description "[Huntington's disease (HD) is a dominant neurodegenerative disorder that is due to expansion of an unstable HTT CAG repeat for which genome-wide genetic scans are now revealing chromosome regions that contain disease-modifying genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1260496.RAykUk60OL5Iy0e097zrfzyhdSFP_jmV4kOcPcxx2Zm7M130_provenance.