Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_provenance.
- NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_assertion description "[Structural and polymorphic variations in Neuregulin 3 (NRG3), 10q22-23 are associated with a broad spectrum of neurodevelopmental disorders including developmental delay, cognitive impairment, autism, and schizophrenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_provenance.
- NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_assertion evidence source_evidence_curated NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_provenance.
- NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_assertion SIO_000772 20713722 NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_provenance.
- NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_assertion wasDerivedFrom ctd_human-20130708 NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_provenance.
- NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_assertion wasGeneratedBy ECO_0000218 NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_provenance.
- ctd_human-20130708 importedOn "2013-07-24" NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_provenance.