Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_assertion type Assertion NP24838.RA7M9IFZFGsIBnjVbtZLn-iG5BwKgaI4TTStkoklrLp08130_head.
- 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.