Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_provenance.
- NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_assertion wasGeneratedBy ECO_0000203 NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_provenance.
- NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_assertion wasDerivedFrom befree-20140225 NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_provenance.
- NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_assertion SIO_000772 20844025 NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_provenance.
- NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_assertion evidence source_evidence_literature NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_provenance.
- NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_assertion description "[We studied an adult patient with ORD due to homozygous POR A287P, the most frequent POR mutation in Caucasians, and her clinically unaffected, heterozygous mother.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_provenance.
- befree-20140225 importedOn "2014-02-25" NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_provenance.