Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP525563.RAyeQhGWbIvnyFHkNyxHjzR4vAh7qAPT4vTjBZCxuUBHQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP525563.RAyeQhGWbIvnyFHkNyxHjzR4vAh7qAPT4vTjBZCxuUBHQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP525563.RAyeQhGWbIvnyFHkNyxHjzR4vAh7qAPT4vTjBZCxuUBHQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP525563.RAyeQhGWbIvnyFHkNyxHjzR4vAh7qAPT4vTjBZCxuUBHQ130_provenance.
- NP525563.RAyeQhGWbIvnyFHkNyxHjzR4vAh7qAPT4vTjBZCxuUBHQ130_assertion description "[This study provides new data supporting two distinct but overlapping pathways in OGCT development; one involving spontaneous KIT mutation(s) leading to increased survival and proliferation of undifferentiated oogonia, the other related to presence of Y chromosome material and ensuing gonadal dysgenesis in phenotypic females.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP525563.RAyeQhGWbIvnyFHkNyxHjzR4vAh7qAPT4vTjBZCxuUBHQ130_provenance.
- NP525563.RAyeQhGWbIvnyFHkNyxHjzR4vAh7qAPT4vTjBZCxuUBHQ130_assertion evidence source_evidence_literature NP525563.RAyeQhGWbIvnyFHkNyxHjzR4vAh7qAPT4vTjBZCxuUBHQ130_provenance.
- NP525563.RAyeQhGWbIvnyFHkNyxHjzR4vAh7qAPT4vTjBZCxuUBHQ130_assertion SIO_000772 17274819 NP525563.RAyeQhGWbIvnyFHkNyxHjzR4vAh7qAPT4vTjBZCxuUBHQ130_provenance.
- NP525563.RAyeQhGWbIvnyFHkNyxHjzR4vAh7qAPT4vTjBZCxuUBHQ130_assertion wasDerivedFrom befree-20150227 NP525563.RAyeQhGWbIvnyFHkNyxHjzR4vAh7qAPT4vTjBZCxuUBHQ130_provenance.
- NP525563.RAyeQhGWbIvnyFHkNyxHjzR4vAh7qAPT4vTjBZCxuUBHQ130_assertion wasGeneratedBy ECO_0000203 NP525563.RAyeQhGWbIvnyFHkNyxHjzR4vAh7qAPT4vTjBZCxuUBHQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP525563.RAyeQhGWbIvnyFHkNyxHjzR4vAh7qAPT4vTjBZCxuUBHQ130_provenance.