Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP690035.RA1evgujB1LwqrgNKKNli4tR1BnEJCNt0dCnP-Zui-7Hk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP690035.RA1evgujB1LwqrgNKKNli4tR1BnEJCNt0dCnP-Zui-7Hk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690035.RA1evgujB1LwqrgNKKNli4tR1BnEJCNt0dCnP-Zui-7Hk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690035.RA1evgujB1LwqrgNKKNli4tR1BnEJCNt0dCnP-Zui-7Hk130_provenance.
- NP690035.RA1evgujB1LwqrgNKKNli4tR1BnEJCNt0dCnP-Zui-7Hk130_assertion description "[In these cases, mutational analysis of the GCH1 gene is an alternative to diagnose DRD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690035.RA1evgujB1LwqrgNKKNli4tR1BnEJCNt0dCnP-Zui-7Hk130_provenance.
- NP690035.RA1evgujB1LwqrgNKKNli4tR1BnEJCNt0dCnP-Zui-7Hk130_assertion evidence source_evidence_literature NP690035.RA1evgujB1LwqrgNKKNli4tR1BnEJCNt0dCnP-Zui-7Hk130_provenance.
- NP690035.RA1evgujB1LwqrgNKKNli4tR1BnEJCNt0dCnP-Zui-7Hk130_assertion SIO_000772 18752196 NP690035.RA1evgujB1LwqrgNKKNli4tR1BnEJCNt0dCnP-Zui-7Hk130_provenance.
- NP690035.RA1evgujB1LwqrgNKKNli4tR1BnEJCNt0dCnP-Zui-7Hk130_assertion wasDerivedFrom befree-2016 NP690035.RA1evgujB1LwqrgNKKNli4tR1BnEJCNt0dCnP-Zui-7Hk130_provenance.
- NP690035.RA1evgujB1LwqrgNKKNli4tR1BnEJCNt0dCnP-Zui-7Hk130_assertion wasGeneratedBy ECO_0000203 NP690035.RA1evgujB1LwqrgNKKNli4tR1BnEJCNt0dCnP-Zui-7Hk130_provenance.
- befree-2016 importedOn "2016-02-19" NP690035.RA1evgujB1LwqrgNKKNli4tR1BnEJCNt0dCnP-Zui-7Hk130_provenance.