Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_provenance.
- 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.
- gad-20150221 importedOn "2015-02-21" NP55170.RAq5KmUxMHc7-ioHB8ZlxBuTNBVDCTvlGAnjZg27VTmOs130_provenance.