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- source_evidence_literature type ECO_0000212 NP341221.RAZb9NfVJyzyo-nJuUP0IfKZHBRJi6nanVadYREDO3NZI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP341221.RAZb9NfVJyzyo-nJuUP0IfKZHBRJi6nanVadYREDO3NZI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP341221.RAZb9NfVJyzyo-nJuUP0IfKZHBRJi6nanVadYREDO3NZI130_provenance.
- NP341221.RAZb9NfVJyzyo-nJuUP0IfKZHBRJi6nanVadYREDO3NZI130_assertion description "[Recently, mutations in the electron donor enzyme P450 oxidoreductase were identified as the cause of CAH with apparent combined 17alpha-hydroxylase and 21-hydroxylase deficiency, thereby illustrating the impact of redox regulation enzymes on steroidogenesis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP341221.RAZb9NfVJyzyo-nJuUP0IfKZHBRJi6nanVadYREDO3NZI130_provenance.
- NP341221.RAZb9NfVJyzyo-nJuUP0IfKZHBRJi6nanVadYREDO3NZI130_assertion evidence source_evidence_literature NP341221.RAZb9NfVJyzyo-nJuUP0IfKZHBRJi6nanVadYREDO3NZI130_provenance.
- NP341221.RAZb9NfVJyzyo-nJuUP0IfKZHBRJi6nanVadYREDO3NZI130_assertion SIO_000772 17223983 NP341221.RAZb9NfVJyzyo-nJuUP0IfKZHBRJi6nanVadYREDO3NZI130_provenance.
- NP341221.RAZb9NfVJyzyo-nJuUP0IfKZHBRJi6nanVadYREDO3NZI130_assertion wasDerivedFrom befree-20150227 NP341221.RAZb9NfVJyzyo-nJuUP0IfKZHBRJi6nanVadYREDO3NZI130_provenance.
- NP341221.RAZb9NfVJyzyo-nJuUP0IfKZHBRJi6nanVadYREDO3NZI130_assertion wasGeneratedBy ECO_0000203 NP341221.RAZb9NfVJyzyo-nJuUP0IfKZHBRJi6nanVadYREDO3NZI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP341221.RAZb9NfVJyzyo-nJuUP0IfKZHBRJi6nanVadYREDO3NZI130_provenance.