Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP186178.RAJfY9s3Ju2VSL-Y022BCSuH6sPaxgatSREhD_kcPX_30130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP186178.RAJfY9s3Ju2VSL-Y022BCSuH6sPaxgatSREhD_kcPX_30130_assertion type Assertion NP186178.RAJfY9s3Ju2VSL-Y022BCSuH6sPaxgatSREhD_kcPX_30130_head.
- NP186178.RAJfY9s3Ju2VSL-Y022BCSuH6sPaxgatSREhD_kcPX_30130_assertion description "[We studied membrane binding and enzyme function of six variant forms of human steroid 21-hydroxylase (P450c21), a mutant (P30Q) from a patient with congenital adrenal hyperplasia, four artificial deletions in the amino terminal region (delS1 and del S2; the first and second hydrophobic segment, delS3; the region in between, delS4; the combination of these), and one naturally ocurring polymorphism in a region implicated to be critical for membrane integration (delL10).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP186178.RAJfY9s3Ju2VSL-Y022BCSuH6sPaxgatSREhD_kcPX_30130_provenance.
- NP186178.RAJfY9s3Ju2VSL-Y022BCSuH6sPaxgatSREhD_kcPX_30130_assertion evidence source_evidence_literature NP186178.RAJfY9s3Ju2VSL-Y022BCSuH6sPaxgatSREhD_kcPX_30130_provenance.
- NP186178.RAJfY9s3Ju2VSL-Y022BCSuH6sPaxgatSREhD_kcPX_30130_assertion SIO_000772 10198222 NP186178.RAJfY9s3Ju2VSL-Y022BCSuH6sPaxgatSREhD_kcPX_30130_provenance.
- NP186178.RAJfY9s3Ju2VSL-Y022BCSuH6sPaxgatSREhD_kcPX_30130_assertion wasDerivedFrom befree-20140225 NP186178.RAJfY9s3Ju2VSL-Y022BCSuH6sPaxgatSREhD_kcPX_30130_provenance.
- NP186178.RAJfY9s3Ju2VSL-Y022BCSuH6sPaxgatSREhD_kcPX_30130_assertion wasGeneratedBy ECO_0000203 NP186178.RAJfY9s3Ju2VSL-Y022BCSuH6sPaxgatSREhD_kcPX_30130_provenance.