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- source_evidence_literature type ECO_0000212 NP278611.RAAsmti6KJHfD8nn7YDR53ohh29cmM-ZhzGj_P--CQMuc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP278611.RAAsmti6KJHfD8nn7YDR53ohh29cmM-ZhzGj_P--CQMuc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP278611.RAAsmti6KJHfD8nn7YDR53ohh29cmM-ZhzGj_P--CQMuc130_provenance.
- NP278611.RAAsmti6KJHfD8nn7YDR53ohh29cmM-ZhzGj_P--CQMuc130_assertion description "[PROP1 gene mutations lead to combined pituitary deficiency, and HESX gene mutations result in septo-optic dysplasia, both of which include HH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP278611.RAAsmti6KJHfD8nn7YDR53ohh29cmM-ZhzGj_P--CQMuc130_provenance.
- NP278611.RAAsmti6KJHfD8nn7YDR53ohh29cmM-ZhzGj_P--CQMuc130_assertion evidence source_evidence_literature NP278611.RAAsmti6KJHfD8nn7YDR53ohh29cmM-ZhzGj_P--CQMuc130_provenance.
- NP278611.RAAsmti6KJHfD8nn7YDR53ohh29cmM-ZhzGj_P--CQMuc130_assertion SIO_000772 10727999 NP278611.RAAsmti6KJHfD8nn7YDR53ohh29cmM-ZhzGj_P--CQMuc130_provenance.
- NP278611.RAAsmti6KJHfD8nn7YDR53ohh29cmM-ZhzGj_P--CQMuc130_assertion wasDerivedFrom befree-2016 NP278611.RAAsmti6KJHfD8nn7YDR53ohh29cmM-ZhzGj_P--CQMuc130_provenance.
- NP278611.RAAsmti6KJHfD8nn7YDR53ohh29cmM-ZhzGj_P--CQMuc130_assertion wasGeneratedBy ECO_0000203 NP278611.RAAsmti6KJHfD8nn7YDR53ohh29cmM-ZhzGj_P--CQMuc130_provenance.
- befree-2016 importedOn "2016-02-19" NP278611.RAAsmti6KJHfD8nn7YDR53ohh29cmM-ZhzGj_P--CQMuc130_provenance.