Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP54652.RAgxhQ0wqwvnfOKJjv90PCSS_1yy5rEaj2QOCbyKFY0-k130_assertion> ?p ?o ?g. }
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- NP54652.RAgxhQ0wqwvnfOKJjv90PCSS_1yy5rEaj2QOCbyKFY0-k130_assertion type Assertion NP54652.RAgxhQ0wqwvnfOKJjv90PCSS_1yy5rEaj2QOCbyKFY0-k130_head.
- NP54652.RAgxhQ0wqwvnfOKJjv90PCSS_1yy5rEaj2QOCbyKFY0-k130_assertion description "[Common genetic variants on 1p13.2 associate with risk of autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP54652.RAgxhQ0wqwvnfOKJjv90PCSS_1yy5rEaj2QOCbyKFY0-k130_provenance.
- NP54652.RAgxhQ0wqwvnfOKJjv90PCSS_1yy5rEaj2QOCbyKFY0-k130_assertion evidence source_evidence_curated NP54652.RAgxhQ0wqwvnfOKJjv90PCSS_1yy5rEaj2QOCbyKFY0-k130_provenance.
- NP54652.RAgxhQ0wqwvnfOKJjv90PCSS_1yy5rEaj2QOCbyKFY0-k130_assertion SIO_000772 24189344 NP54652.RAgxhQ0wqwvnfOKJjv90PCSS_1yy5rEaj2QOCbyKFY0-k130_provenance.
- NP54652.RAgxhQ0wqwvnfOKJjv90PCSS_1yy5rEaj2QOCbyKFY0-k130_assertion wasDerivedFrom gwascat-2016 NP54652.RAgxhQ0wqwvnfOKJjv90PCSS_1yy5rEaj2QOCbyKFY0-k130_provenance.
- NP54652.RAgxhQ0wqwvnfOKJjv90PCSS_1yy5rEaj2QOCbyKFY0-k130_assertion wasGeneratedBy ECO_0000218 NP54652.RAgxhQ0wqwvnfOKJjv90PCSS_1yy5rEaj2QOCbyKFY0-k130_provenance.