Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_assertion type Assertion NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_head.
- NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_assertion description "[Context: Steroid 21-hydroxylase deficiency is the most common enzymatic defect causing congenital adrenal hyperplasia with genotype/phenotype relationships for common mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_provenance.
- NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_assertion evidence source_evidence_literature NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_provenance.
- NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_assertion SIO_000772 20080860 NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_provenance.
- NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_assertion wasDerivedFrom gad-20150221 NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_provenance.
- NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_assertion wasGeneratedBy ECO_0000203 NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_provenance.