Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1039806.RAO9lLXACPeU-5Z31T-qXW7czj8iGAmJTg1QtJOzs0yzw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1039806.RAO9lLXACPeU-5Z31T-qXW7czj8iGAmJTg1QtJOzs0yzw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1039806.RAO9lLXACPeU-5Z31T-qXW7czj8iGAmJTg1QtJOzs0yzw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1039806.RAO9lLXACPeU-5Z31T-qXW7czj8iGAmJTg1QtJOzs0yzw130_provenance.
- NP1039806.RAO9lLXACPeU-5Z31T-qXW7czj8iGAmJTg1QtJOzs0yzw130_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." NP1039806.RAO9lLXACPeU-5Z31T-qXW7czj8iGAmJTg1QtJOzs0yzw130_provenance.
- NP1039806.RAO9lLXACPeU-5Z31T-qXW7czj8iGAmJTg1QtJOzs0yzw130_assertion evidence source_evidence_literature NP1039806.RAO9lLXACPeU-5Z31T-qXW7czj8iGAmJTg1QtJOzs0yzw130_provenance.
- NP1039806.RAO9lLXACPeU-5Z31T-qXW7czj8iGAmJTg1QtJOzs0yzw130_assertion SIO_000772 23279116 NP1039806.RAO9lLXACPeU-5Z31T-qXW7czj8iGAmJTg1QtJOzs0yzw130_provenance.
- NP1039806.RAO9lLXACPeU-5Z31T-qXW7czj8iGAmJTg1QtJOzs0yzw130_assertion wasDerivedFrom befree-2016 NP1039806.RAO9lLXACPeU-5Z31T-qXW7czj8iGAmJTg1QtJOzs0yzw130_provenance.
- NP1039806.RAO9lLXACPeU-5Z31T-qXW7czj8iGAmJTg1QtJOzs0yzw130_assertion wasGeneratedBy ECO_0000203 NP1039806.RAO9lLXACPeU-5Z31T-qXW7czj8iGAmJTg1QtJOzs0yzw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1039806.RAO9lLXACPeU-5Z31T-qXW7czj8iGAmJTg1QtJOzs0yzw130_provenance.