Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1372365.RAz1PrMMCvndc-KF3V7Z9N9R1HweM572z2YhxHz5WNTJE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1372365.RAz1PrMMCvndc-KF3V7Z9N9R1HweM572z2YhxHz5WNTJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1372365.RAz1PrMMCvndc-KF3V7Z9N9R1HweM572z2YhxHz5WNTJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1372365.RAz1PrMMCvndc-KF3V7Z9N9R1HweM572z2YhxHz5WNTJE130_provenance.
- NP1372365.RAz1PrMMCvndc-KF3V7Z9N9R1HweM572z2YhxHz5WNTJE130_assertion description "[Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1372365.RAz1PrMMCvndc-KF3V7Z9N9R1HweM572z2YhxHz5WNTJE130_provenance.
- NP1372365.RAz1PrMMCvndc-KF3V7Z9N9R1HweM572z2YhxHz5WNTJE130_assertion evidence source_evidence_literature NP1372365.RAz1PrMMCvndc-KF3V7Z9N9R1HweM572z2YhxHz5WNTJE130_provenance.
- NP1372365.RAz1PrMMCvndc-KF3V7Z9N9R1HweM572z2YhxHz5WNTJE130_assertion SIO_000772 9140395 NP1372365.RAz1PrMMCvndc-KF3V7Z9N9R1HweM572z2YhxHz5WNTJE130_provenance.
- NP1372365.RAz1PrMMCvndc-KF3V7Z9N9R1HweM572z2YhxHz5WNTJE130_assertion wasDerivedFrom befree-2016 NP1372365.RAz1PrMMCvndc-KF3V7Z9N9R1HweM572z2YhxHz5WNTJE130_provenance.
- NP1372365.RAz1PrMMCvndc-KF3V7Z9N9R1HweM572z2YhxHz5WNTJE130_assertion wasGeneratedBy ECO_0000203 NP1372365.RAz1PrMMCvndc-KF3V7Z9N9R1HweM572z2YhxHz5WNTJE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1372365.RAz1PrMMCvndc-KF3V7Z9N9R1HweM572z2YhxHz5WNTJE130_provenance.