Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP390178.RA47KJNmAw4znH9dBgSw6o-u-wNIzxztSfuDVbQWWEbuU130_assertion> ?p ?o ?g. }
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- NP390178.RA47KJNmAw4znH9dBgSw6o-u-wNIzxztSfuDVbQWWEbuU130_assertion type Assertion NP390178.RA47KJNmAw4znH9dBgSw6o-u-wNIzxztSfuDVbQWWEbuU130_head.
- NP390178.RA47KJNmAw4znH9dBgSw6o-u-wNIzxztSfuDVbQWWEbuU130_assertion description "[Deletion of Xpter encompassing the SHOX gene and PAR1 region in familial patients with Leri-Weill Dyschondrosteosis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP390178.RA47KJNmAw4znH9dBgSw6o-u-wNIzxztSfuDVbQWWEbuU130_provenance.
- NP390178.RA47KJNmAw4znH9dBgSw6o-u-wNIzxztSfuDVbQWWEbuU130_assertion evidence source_evidence_literature NP390178.RA47KJNmAw4znH9dBgSw6o-u-wNIzxztSfuDVbQWWEbuU130_provenance.
- NP390178.RA47KJNmAw4znH9dBgSw6o-u-wNIzxztSfuDVbQWWEbuU130_assertion SIO_000772 19400538 NP390178.RA47KJNmAw4znH9dBgSw6o-u-wNIzxztSfuDVbQWWEbuU130_provenance.
- NP390178.RA47KJNmAw4znH9dBgSw6o-u-wNIzxztSfuDVbQWWEbuU130_assertion wasDerivedFrom befree-20150227 NP390178.RA47KJNmAw4znH9dBgSw6o-u-wNIzxztSfuDVbQWWEbuU130_provenance.
- NP390178.RA47KJNmAw4znH9dBgSw6o-u-wNIzxztSfuDVbQWWEbuU130_assertion wasGeneratedBy ECO_0000203 NP390178.RA47KJNmAw4znH9dBgSw6o-u-wNIzxztSfuDVbQWWEbuU130_provenance.