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- NP26592.RA3zueSfERJ_H7Smju-HfzL8nmfTdMjTt0C4sFHP2ianE130_assertion type Assertion NP26592.RA3zueSfERJ_H7Smju-HfzL8nmfTdMjTt0C4sFHP2ianE130_head.
- NP26592.RA3zueSfERJ_H7Smju-HfzL8nmfTdMjTt0C4sFHP2ianE130_assertion wasGeneratedBy ECO_0000218 NP26592.RA3zueSfERJ_H7Smju-HfzL8nmfTdMjTt0C4sFHP2ianE130_provenance.
- NP26592.RA3zueSfERJ_H7Smju-HfzL8nmfTdMjTt0C4sFHP2ianE130_assertion wasDerivedFrom ctd_human-2016 NP26592.RA3zueSfERJ_H7Smju-HfzL8nmfTdMjTt0C4sFHP2ianE130_provenance.
- NP26592.RA3zueSfERJ_H7Smju-HfzL8nmfTdMjTt0C4sFHP2ianE130_assertion SIO_000772 20663923 NP26592.RA3zueSfERJ_H7Smju-HfzL8nmfTdMjTt0C4sFHP2ianE130_provenance.
- NP26592.RA3zueSfERJ_H7Smju-HfzL8nmfTdMjTt0C4sFHP2ianE130_assertion evidence source_evidence_curated NP26592.RA3zueSfERJ_H7Smju-HfzL8nmfTdMjTt0C4sFHP2ianE130_provenance.
- NP26592.RA3zueSfERJ_H7Smju-HfzL8nmfTdMjTt0C4sFHP2ianE130_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." NP26592.RA3zueSfERJ_H7Smju-HfzL8nmfTdMjTt0C4sFHP2ianE130_provenance.