Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP842718.RAOiF3F3RrR66xGWT3D6j0YhnJdp0LSvw0ZmTs1FUQyhE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP842718.RAOiF3F3RrR66xGWT3D6j0YhnJdp0LSvw0ZmTs1FUQyhE130_assertion type Assertion NP842718.RAOiF3F3RrR66xGWT3D6j0YhnJdp0LSvw0ZmTs1FUQyhE130_head.
- NP842718.RAOiF3F3RrR66xGWT3D6j0YhnJdp0LSvw0ZmTs1FUQyhE130_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." NP842718.RAOiF3F3RrR66xGWT3D6j0YhnJdp0LSvw0ZmTs1FUQyhE130_provenance.
- NP842718.RAOiF3F3RrR66xGWT3D6j0YhnJdp0LSvw0ZmTs1FUQyhE130_assertion evidence source_evidence_literature NP842718.RAOiF3F3RrR66xGWT3D6j0YhnJdp0LSvw0ZmTs1FUQyhE130_provenance.
- NP842718.RAOiF3F3RrR66xGWT3D6j0YhnJdp0LSvw0ZmTs1FUQyhE130_assertion SIO_000772 17223983 NP842718.RAOiF3F3RrR66xGWT3D6j0YhnJdp0LSvw0ZmTs1FUQyhE130_provenance.
- NP842718.RAOiF3F3RrR66xGWT3D6j0YhnJdp0LSvw0ZmTs1FUQyhE130_assertion wasDerivedFrom befree-20140225 NP842718.RAOiF3F3RrR66xGWT3D6j0YhnJdp0LSvw0ZmTs1FUQyhE130_provenance.
- NP842718.RAOiF3F3RrR66xGWT3D6j0YhnJdp0LSvw0ZmTs1FUQyhE130_assertion wasGeneratedBy ECO_0000203 NP842718.RAOiF3F3RrR66xGWT3D6j0YhnJdp0LSvw0ZmTs1FUQyhE130_provenance.