Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP588854.RAzQdzZjruGR1Y-ownC0NrQD28negMqxOqg7mkmrz3j8I130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP588854.RAzQdzZjruGR1Y-ownC0NrQD28negMqxOqg7mkmrz3j8I130_assertion type Assertion NP588854.RAzQdzZjruGR1Y-ownC0NrQD28negMqxOqg7mkmrz3j8I130_head.
- NP588854.RAzQdzZjruGR1Y-ownC0NrQD28negMqxOqg7mkmrz3j8I130_assertion description "[P450 oxidoreductase deficiency (ORD) has a complex phenotype including two unique features not observed in any other CAH variant, skeletal malformations and severe genital ambiguity in both sexes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588854.RAzQdzZjruGR1Y-ownC0NrQD28negMqxOqg7mkmrz3j8I130_provenance.
- NP588854.RAzQdzZjruGR1Y-ownC0NrQD28negMqxOqg7mkmrz3j8I130_assertion evidence source_evidence_literature NP588854.RAzQdzZjruGR1Y-ownC0NrQD28negMqxOqg7mkmrz3j8I130_provenance.
- NP588854.RAzQdzZjruGR1Y-ownC0NrQD28negMqxOqg7mkmrz3j8I130_assertion SIO_000772 17223983 NP588854.RAzQdzZjruGR1Y-ownC0NrQD28negMqxOqg7mkmrz3j8I130_provenance.
- NP588854.RAzQdzZjruGR1Y-ownC0NrQD28negMqxOqg7mkmrz3j8I130_assertion wasDerivedFrom befree-2016 NP588854.RAzQdzZjruGR1Y-ownC0NrQD28negMqxOqg7mkmrz3j8I130_provenance.
- NP588854.RAzQdzZjruGR1Y-ownC0NrQD28negMqxOqg7mkmrz3j8I130_assertion wasGeneratedBy ECO_0000203 NP588854.RAzQdzZjruGR1Y-ownC0NrQD28negMqxOqg7mkmrz3j8I130_provenance.