Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP724202.RAVaRf6RXqfryXy_zgkLX81D-gxmIQklVfCx9emLB0QOY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP724202.RAVaRf6RXqfryXy_zgkLX81D-gxmIQklVfCx9emLB0QOY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP724202.RAVaRf6RXqfryXy_zgkLX81D-gxmIQklVfCx9emLB0QOY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP724202.RAVaRf6RXqfryXy_zgkLX81D-gxmIQklVfCx9emLB0QOY130_provenance.
- NP724202.RAVaRf6RXqfryXy_zgkLX81D-gxmIQklVfCx9emLB0QOY130_assertion description "[SRD5A2 gene mutations may not be as infrequent as previously considered in 46,XY DSD patients with variable degrees of external genitalia virilization at birth and normal T production and appears to be the second aetiology in our series.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP724202.RAVaRf6RXqfryXy_zgkLX81D-gxmIQklVfCx9emLB0QOY130_provenance.
- NP724202.RAVaRf6RXqfryXy_zgkLX81D-gxmIQklVfCx9emLB0QOY130_assertion evidence source_evidence_literature NP724202.RAVaRf6RXqfryXy_zgkLX81D-gxmIQklVfCx9emLB0QOY130_provenance.
- NP724202.RAVaRf6RXqfryXy_zgkLX81D-gxmIQklVfCx9emLB0QOY130_assertion SIO_000772 21631525 NP724202.RAVaRf6RXqfryXy_zgkLX81D-gxmIQklVfCx9emLB0QOY130_provenance.
- NP724202.RAVaRf6RXqfryXy_zgkLX81D-gxmIQklVfCx9emLB0QOY130_assertion wasDerivedFrom befree-20140225 NP724202.RAVaRf6RXqfryXy_zgkLX81D-gxmIQklVfCx9emLB0QOY130_provenance.
- NP724202.RAVaRf6RXqfryXy_zgkLX81D-gxmIQklVfCx9emLB0QOY130_assertion wasGeneratedBy ECO_0000203 NP724202.RAVaRf6RXqfryXy_zgkLX81D-gxmIQklVfCx9emLB0QOY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP724202.RAVaRf6RXqfryXy_zgkLX81D-gxmIQklVfCx9emLB0QOY130_provenance.