Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP2255.RAmHRmiH2GCvta-Fqi8Qg28EnkczspCp0qFTm-NK2xryw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_curated type ECO_0000205 NP2255.RAmHRmiH2GCvta-Fqi8Qg28EnkczspCp0qFTm-NK2xryw130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP2255.RAmHRmiH2GCvta-Fqi8Qg28EnkczspCp0qFTm-NK2xryw130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP2255.RAmHRmiH2GCvta-Fqi8Qg28EnkczspCp0qFTm-NK2xryw130_provenance.
- NP2255.RAmHRmiH2GCvta-Fqi8Qg28EnkczspCp0qFTm-NK2xryw130_assertion wasGeneratedBy ECO_0000218 NP2255.RAmHRmiH2GCvta-Fqi8Qg28EnkczspCp0qFTm-NK2xryw130_provenance.
- NP2255.RAmHRmiH2GCvta-Fqi8Qg28EnkczspCp0qFTm-NK2xryw130_assertion wasDerivedFrom uniprot-20130724 NP2255.RAmHRmiH2GCvta-Fqi8Qg28EnkczspCp0qFTm-NK2xryw130_provenance.
- NP2255.RAmHRmiH2GCvta-Fqi8Qg28EnkczspCp0qFTm-NK2xryw130_assertion SIO_000772 15605412 NP2255.RAmHRmiH2GCvta-Fqi8Qg28EnkczspCp0qFTm-NK2xryw130_provenance.
- NP2255.RAmHRmiH2GCvta-Fqi8Qg28EnkczspCp0qFTm-NK2xryw130_assertion evidence source_evidence_curated NP2255.RAmHRmiH2GCvta-Fqi8Qg28EnkczspCp0qFTm-NK2xryw130_provenance.
- NP2255.RAmHRmiH2GCvta-Fqi8Qg28EnkczspCp0qFTm-NK2xryw130_assertion description "[KAL is genetically heterogeneous and two genes have so far been identified, namely KAL1 (Xp22.3) and FGFR1/KAL2 (8p12), which underlie the X chromosome-linked form and an autosomal dominant form of the disease, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2255.RAmHRmiH2GCvta-Fqi8Qg28EnkczspCp0qFTm-NK2xryw130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP2255.RAmHRmiH2GCvta-Fqi8Qg28EnkczspCp0qFTm-NK2xryw130_provenance.