Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP713103.RAFomCFQsxcvn4sRWWCpkqr9bGQRr2WJwT5PXeOMR7iHU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP713103.RAFomCFQsxcvn4sRWWCpkqr9bGQRr2WJwT5PXeOMR7iHU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP713103.RAFomCFQsxcvn4sRWWCpkqr9bGQRr2WJwT5PXeOMR7iHU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP713103.RAFomCFQsxcvn4sRWWCpkqr9bGQRr2WJwT5PXeOMR7iHU130_provenance.
- NP713103.RAFomCFQsxcvn4sRWWCpkqr9bGQRr2WJwT5PXeOMR7iHU130_assertion description "[In this report we present clinical, cytogenetic, and molecular-cytogenetic data of a patient with ambiguous genitalia and true hermaphroditism, who had a unique mosaic karyotype, comprising three different cell lines: 46,XX(SRY+), 45,X(SRY+), and 45,X.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP713103.RAFomCFQsxcvn4sRWWCpkqr9bGQRr2WJwT5PXeOMR7iHU130_provenance.
- NP713103.RAFomCFQsxcvn4sRWWCpkqr9bGQRr2WJwT5PXeOMR7iHU130_assertion evidence source_evidence_literature NP713103.RAFomCFQsxcvn4sRWWCpkqr9bGQRr2WJwT5PXeOMR7iHU130_provenance.
- NP713103.RAFomCFQsxcvn4sRWWCpkqr9bGQRr2WJwT5PXeOMR7iHU130_assertion SIO_000772 12503111 NP713103.RAFomCFQsxcvn4sRWWCpkqr9bGQRr2WJwT5PXeOMR7iHU130_provenance.
- NP713103.RAFomCFQsxcvn4sRWWCpkqr9bGQRr2WJwT5PXeOMR7iHU130_assertion wasDerivedFrom befree-20150227 NP713103.RAFomCFQsxcvn4sRWWCpkqr9bGQRr2WJwT5PXeOMR7iHU130_provenance.
- NP713103.RAFomCFQsxcvn4sRWWCpkqr9bGQRr2WJwT5PXeOMR7iHU130_assertion wasGeneratedBy ECO_0000203 NP713103.RAFomCFQsxcvn4sRWWCpkqr9bGQRr2WJwT5PXeOMR7iHU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP713103.RAFomCFQsxcvn4sRWWCpkqr9bGQRr2WJwT5PXeOMR7iHU130_provenance.