Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1376389.RABRVwMpaEgHjfs4Ii6V-mA7ShA1HAwSW2n-LzZZ_n9Wc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1376389.RABRVwMpaEgHjfs4Ii6V-mA7ShA1HAwSW2n-LzZZ_n9Wc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1376389.RABRVwMpaEgHjfs4Ii6V-mA7ShA1HAwSW2n-LzZZ_n9Wc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1376389.RABRVwMpaEgHjfs4Ii6V-mA7ShA1HAwSW2n-LzZZ_n9Wc130_provenance.
- befree-2016 importedOn "2016-02-19" NP1376389.RABRVwMpaEgHjfs4Ii6V-mA7ShA1HAwSW2n-LzZZ_n9Wc130_provenance.
- NP1376389.RABRVwMpaEgHjfs4Ii6V-mA7ShA1HAwSW2n-LzZZ_n9Wc130_assertion wasGeneratedBy ECO_0000203 NP1376389.RABRVwMpaEgHjfs4Ii6V-mA7ShA1HAwSW2n-LzZZ_n9Wc130_provenance.
- NP1376389.RABRVwMpaEgHjfs4Ii6V-mA7ShA1HAwSW2n-LzZZ_n9Wc130_assertion wasDerivedFrom befree-2016 NP1376389.RABRVwMpaEgHjfs4Ii6V-mA7ShA1HAwSW2n-LzZZ_n9Wc130_provenance.
- NP1376389.RABRVwMpaEgHjfs4Ii6V-mA7ShA1HAwSW2n-LzZZ_n9Wc130_assertion SIO_000772 9215316 NP1376389.RABRVwMpaEgHjfs4Ii6V-mA7ShA1HAwSW2n-LzZZ_n9Wc130_provenance.
- NP1376389.RABRVwMpaEgHjfs4Ii6V-mA7ShA1HAwSW2n-LzZZ_n9Wc130_assertion evidence source_evidence_literature NP1376389.RABRVwMpaEgHjfs4Ii6V-mA7ShA1HAwSW2n-LzZZ_n9Wc130_provenance.
- NP1376389.RABRVwMpaEgHjfs4Ii6V-mA7ShA1HAwSW2n-LzZZ_n9Wc130_assertion description "[Therefore, we investigated both the cytochrome P450scc and StAR genes in a Korean family with a fairly mild form of lipoid CAH to identify the mutation(s) causing this disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1376389.RABRVwMpaEgHjfs4Ii6V-mA7ShA1HAwSW2n-LzZZ_n9Wc130_provenance.