Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP713137.RAi24nkQfnDrMh1MH2bPHLf3Qf4DstDa-ZRLz-GsVq6Nc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP713137.RAi24nkQfnDrMh1MH2bPHLf3Qf4DstDa-ZRLz-GsVq6Nc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP713137.RAi24nkQfnDrMh1MH2bPHLf3Qf4DstDa-ZRLz-GsVq6Nc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP713137.RAi24nkQfnDrMh1MH2bPHLf3Qf4DstDa-ZRLz-GsVq6Nc130_provenance.
- NP713137.RAi24nkQfnDrMh1MH2bPHLf3Qf4DstDa-ZRLz-GsVq6Nc130_assertion description "[Numerical and structural chromosomal abnormalities were noted in 115 (34.0%) patients which included 45,X Turner syndrome (10.7%), Turner syndrome variants (13.9%), XY females (6.5%), 45,X/46,XY (0.9%), 46,XX/46,XY (0.6%), 47,XXX (0.3%), 47,XX,+ mar (0.3%), 46,X,i(X)(p10) (0.3%), 46,XX with SRY gene translocation on X chromosome (0.3%) and 46,XX,inv(7)(p10;q11.2) (0.3%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713137.RAi24nkQfnDrMh1MH2bPHLf3Qf4DstDa-ZRLz-GsVq6Nc130_provenance.
- NP713137.RAi24nkQfnDrMh1MH2bPHLf3Qf4DstDa-ZRLz-GsVq6Nc130_assertion evidence source_evidence_literature NP713137.RAi24nkQfnDrMh1MH2bPHLf3Qf4DstDa-ZRLz-GsVq6Nc130_provenance.
- NP713137.RAi24nkQfnDrMh1MH2bPHLf3Qf4DstDa-ZRLz-GsVq6Nc130_assertion SIO_000772 23279116 NP713137.RAi24nkQfnDrMh1MH2bPHLf3Qf4DstDa-ZRLz-GsVq6Nc130_provenance.
- NP713137.RAi24nkQfnDrMh1MH2bPHLf3Qf4DstDa-ZRLz-GsVq6Nc130_assertion wasDerivedFrom befree-20150227 NP713137.RAi24nkQfnDrMh1MH2bPHLf3Qf4DstDa-ZRLz-GsVq6Nc130_provenance.
- NP713137.RAi24nkQfnDrMh1MH2bPHLf3Qf4DstDa-ZRLz-GsVq6Nc130_assertion wasGeneratedBy ECO_0000203 NP713137.RAi24nkQfnDrMh1MH2bPHLf3Qf4DstDa-ZRLz-GsVq6Nc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP713137.RAi24nkQfnDrMh1MH2bPHLf3Qf4DstDa-ZRLz-GsVq6Nc130_provenance.