Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1336922.RA5ANbnJPW1jnJFcuoYNQtVds9RW0O2SHqRcpSuPLNu1E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1336922.RA5ANbnJPW1jnJFcuoYNQtVds9RW0O2SHqRcpSuPLNu1E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1336922.RA5ANbnJPW1jnJFcuoYNQtVds9RW0O2SHqRcpSuPLNu1E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1336922.RA5ANbnJPW1jnJFcuoYNQtVds9RW0O2SHqRcpSuPLNu1E130_provenance.
- NP1336922.RA5ANbnJPW1jnJFcuoYNQtVds9RW0O2SHqRcpSuPLNu1E130_assertion description "[Approaches for evaluating SRY as a candidate for TDF included the finding of mutations in SRY in the genomes of patients with failed testis development (XY females or 46,XY gonadal dysgenesis) and the production of female to male sex reversed mice transgenic for the mouse homologue of SRY, [Sry].]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1336922.RA5ANbnJPW1jnJFcuoYNQtVds9RW0O2SHqRcpSuPLNu1E130_provenance.
- NP1336922.RA5ANbnJPW1jnJFcuoYNQtVds9RW0O2SHqRcpSuPLNu1E130_assertion evidence source_evidence_literature NP1336922.RA5ANbnJPW1jnJFcuoYNQtVds9RW0O2SHqRcpSuPLNu1E130_provenance.
- NP1336922.RA5ANbnJPW1jnJFcuoYNQtVds9RW0O2SHqRcpSuPLNu1E130_assertion SIO_000772 8257986 NP1336922.RA5ANbnJPW1jnJFcuoYNQtVds9RW0O2SHqRcpSuPLNu1E130_provenance.
- NP1336922.RA5ANbnJPW1jnJFcuoYNQtVds9RW0O2SHqRcpSuPLNu1E130_assertion wasDerivedFrom befree-2016 NP1336922.RA5ANbnJPW1jnJFcuoYNQtVds9RW0O2SHqRcpSuPLNu1E130_provenance.
- NP1336922.RA5ANbnJPW1jnJFcuoYNQtVds9RW0O2SHqRcpSuPLNu1E130_assertion wasGeneratedBy ECO_0000203 NP1336922.RA5ANbnJPW1jnJFcuoYNQtVds9RW0O2SHqRcpSuPLNu1E130_provenance.
- befree-2016 importedOn "2016-02-19" NP1336922.RA5ANbnJPW1jnJFcuoYNQtVds9RW0O2SHqRcpSuPLNu1E130_provenance.