Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP344128.RA3TdVHLLPvsg2AxtL9TXXsB1oYkhHPRJKoi4N2zDaFoo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP344128.RA3TdVHLLPvsg2AxtL9TXXsB1oYkhHPRJKoi4N2zDaFoo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP344128.RA3TdVHLLPvsg2AxtL9TXXsB1oYkhHPRJKoi4N2zDaFoo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP344128.RA3TdVHLLPvsg2AxtL9TXXsB1oYkhHPRJKoi4N2zDaFoo130_provenance.
- NP344128.RA3TdVHLLPvsg2AxtL9TXXsB1oYkhHPRJKoi4N2zDaFoo130_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." NP344128.RA3TdVHLLPvsg2AxtL9TXXsB1oYkhHPRJKoi4N2zDaFoo130_provenance.
- NP344128.RA3TdVHLLPvsg2AxtL9TXXsB1oYkhHPRJKoi4N2zDaFoo130_assertion evidence source_evidence_literature NP344128.RA3TdVHLLPvsg2AxtL9TXXsB1oYkhHPRJKoi4N2zDaFoo130_provenance.
- NP344128.RA3TdVHLLPvsg2AxtL9TXXsB1oYkhHPRJKoi4N2zDaFoo130_assertion SIO_000772 19844114 NP344128.RA3TdVHLLPvsg2AxtL9TXXsB1oYkhHPRJKoi4N2zDaFoo130_provenance.
- NP344128.RA3TdVHLLPvsg2AxtL9TXXsB1oYkhHPRJKoi4N2zDaFoo130_assertion wasDerivedFrom befree-20150227 NP344128.RA3TdVHLLPvsg2AxtL9TXXsB1oYkhHPRJKoi4N2zDaFoo130_provenance.
- NP344128.RA3TdVHLLPvsg2AxtL9TXXsB1oYkhHPRJKoi4N2zDaFoo130_assertion wasGeneratedBy ECO_0000203 NP344128.RA3TdVHLLPvsg2AxtL9TXXsB1oYkhHPRJKoi4N2zDaFoo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP344128.RA3TdVHLLPvsg2AxtL9TXXsB1oYkhHPRJKoi4N2zDaFoo130_provenance.