Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP182388.RAOEtHEjcfl5m7WKoouCs31SapwsffmRjYjxQnHw3kLdA130_assertion> ?p ?o ?g. }
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- NP182388.RAOEtHEjcfl5m7WKoouCs31SapwsffmRjYjxQnHw3kLdA130_assertion type Assertion NP182388.RAOEtHEjcfl5m7WKoouCs31SapwsffmRjYjxQnHw3kLdA130_head.
- NP182388.RAOEtHEjcfl5m7WKoouCs31SapwsffmRjYjxQnHw3kLdA130_assertion wasGeneratedBy ECO_0000203 NP182388.RAOEtHEjcfl5m7WKoouCs31SapwsffmRjYjxQnHw3kLdA130_provenance.
- NP182388.RAOEtHEjcfl5m7WKoouCs31SapwsffmRjYjxQnHw3kLdA130_assertion wasDerivedFrom gad-20150221 NP182388.RAOEtHEjcfl5m7WKoouCs31SapwsffmRjYjxQnHw3kLdA130_provenance.
- NP182388.RAOEtHEjcfl5m7WKoouCs31SapwsffmRjYjxQnHw3kLdA130_assertion SIO_000772 20663923 NP182388.RAOEtHEjcfl5m7WKoouCs31SapwsffmRjYjxQnHw3kLdA130_provenance.
- NP182388.RAOEtHEjcfl5m7WKoouCs31SapwsffmRjYjxQnHw3kLdA130_assertion evidence source_evidence_literature NP182388.RAOEtHEjcfl5m7WKoouCs31SapwsffmRjYjxQnHw3kLdA130_provenance.
- NP182388.RAOEtHEjcfl5m7WKoouCs31SapwsffmRjYjxQnHw3kLdA130_assertion description "[A genome-wide scan for common alleles affecting risk for autism.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP182388.RAOEtHEjcfl5m7WKoouCs31SapwsffmRjYjxQnHw3kLdA130_provenance.