Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP159707.RADnrvwaoKef023QPltYw-WtmM1lcKxNqNNSG8nRNL2MI130_assertion> ?p ?o ?g. }
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- NP159707.RADnrvwaoKef023QPltYw-WtmM1lcKxNqNNSG8nRNL2MI130_assertion type Assertion NP159707.RADnrvwaoKef023QPltYw-WtmM1lcKxNqNNSG8nRNL2MI130_head.
- NP159707.RADnrvwaoKef023QPltYw-WtmM1lcKxNqNNSG8nRNL2MI130_assertion description "[Steroid 11-hydroxylase (CYP11B1) deficiency (11OHD) is the second most common form of congenital adrenal hyperplasia (CAH).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP159707.RADnrvwaoKef023QPltYw-WtmM1lcKxNqNNSG8nRNL2MI130_provenance.
- NP159707.RADnrvwaoKef023QPltYw-WtmM1lcKxNqNNSG8nRNL2MI130_assertion evidence source_evidence_literature NP159707.RADnrvwaoKef023QPltYw-WtmM1lcKxNqNNSG8nRNL2MI130_provenance.
- NP159707.RADnrvwaoKef023QPltYw-WtmM1lcKxNqNNSG8nRNL2MI130_assertion SIO_000772 19844114 NP159707.RADnrvwaoKef023QPltYw-WtmM1lcKxNqNNSG8nRNL2MI130_provenance.
- NP159707.RADnrvwaoKef023QPltYw-WtmM1lcKxNqNNSG8nRNL2MI130_assertion wasDerivedFrom befree-20140225 NP159707.RADnrvwaoKef023QPltYw-WtmM1lcKxNqNNSG8nRNL2MI130_provenance.
- NP159707.RADnrvwaoKef023QPltYw-WtmM1lcKxNqNNSG8nRNL2MI130_assertion wasGeneratedBy ECO_0000203 NP159707.RADnrvwaoKef023QPltYw-WtmM1lcKxNqNNSG8nRNL2MI130_provenance.