Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP131984.RANshiTW80gnruvBheDX38xr3_13ojH-HFffQEZaUsUK8130_assertion> ?p ?o ?g. }
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- NP131984.RANshiTW80gnruvBheDX38xr3_13ojH-HFffQEZaUsUK8130_assertion type Assertion NP131984.RANshiTW80gnruvBheDX38xr3_13ojH-HFffQEZaUsUK8130_head.
- NP131984.RANshiTW80gnruvBheDX38xr3_13ojH-HFffQEZaUsUK8130_assertion wasGeneratedBy ECO_0000203 NP131984.RANshiTW80gnruvBheDX38xr3_13ojH-HFffQEZaUsUK8130_provenance.
- NP131984.RANshiTW80gnruvBheDX38xr3_13ojH-HFffQEZaUsUK8130_assertion wasDerivedFrom gad-20150221 NP131984.RANshiTW80gnruvBheDX38xr3_13ojH-HFffQEZaUsUK8130_provenance.
- NP131984.RANshiTW80gnruvBheDX38xr3_13ojH-HFffQEZaUsUK8130_assertion SIO_000772 20663923 NP131984.RANshiTW80gnruvBheDX38xr3_13ojH-HFffQEZaUsUK8130_provenance.
- NP131984.RANshiTW80gnruvBheDX38xr3_13ojH-HFffQEZaUsUK8130_assertion evidence source_evidence_literature NP131984.RANshiTW80gnruvBheDX38xr3_13ojH-HFffQEZaUsUK8130_provenance.
- NP131984.RANshiTW80gnruvBheDX38xr3_13ojH-HFffQEZaUsUK8130_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." NP131984.RANshiTW80gnruvBheDX38xr3_13ojH-HFffQEZaUsUK8130_provenance.