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- source_evidence_literature type ECO_0000212 NP390178.RA47KJNmAw4znH9dBgSw6o-u-wNIzxztSfuDVbQWWEbuU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP390178.RA47KJNmAw4znH9dBgSw6o-u-wNIzxztSfuDVbQWWEbuU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP390178.RA47KJNmAw4znH9dBgSw6o-u-wNIzxztSfuDVbQWWEbuU130_provenance.
- 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.
- befree-20150227 importedOn "2015-02-27" NP390178.RA47KJNmAw4znH9dBgSw6o-u-wNIzxztSfuDVbQWWEbuU130_provenance.