Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP21381.RA0qaxjRO4B_dNHVtLrf8UbiM3DV2tKZhrefUQKWY2Fos130_assertion> ?p ?o ?g. }
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- NP21381.RA0qaxjRO4B_dNHVtLrf8UbiM3DV2tKZhrefUQKWY2Fos130_assertion type Assertion NP21381.RA0qaxjRO4B_dNHVtLrf8UbiM3DV2tKZhrefUQKWY2Fos130_head.
- NP21381.RA0qaxjRO4B_dNHVtLrf8UbiM3DV2tKZhrefUQKWY2Fos130_assertion wasGeneratedBy ECO_0000218 NP21381.RA0qaxjRO4B_dNHVtLrf8UbiM3DV2tKZhrefUQKWY2Fos130_provenance.
- NP21381.RA0qaxjRO4B_dNHVtLrf8UbiM3DV2tKZhrefUQKWY2Fos130_assertion wasDerivedFrom ctd_human-20150221 NP21381.RA0qaxjRO4B_dNHVtLrf8UbiM3DV2tKZhrefUQKWY2Fos130_provenance.
- NP21381.RA0qaxjRO4B_dNHVtLrf8UbiM3DV2tKZhrefUQKWY2Fos130_assertion SIO_000772 20663923 NP21381.RA0qaxjRO4B_dNHVtLrf8UbiM3DV2tKZhrefUQKWY2Fos130_provenance.
- NP21381.RA0qaxjRO4B_dNHVtLrf8UbiM3DV2tKZhrefUQKWY2Fos130_assertion evidence source_evidence_curated NP21381.RA0qaxjRO4B_dNHVtLrf8UbiM3DV2tKZhrefUQKWY2Fos130_provenance.
- NP21381.RA0qaxjRO4B_dNHVtLrf8UbiM3DV2tKZhrefUQKWY2Fos130_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." NP21381.RA0qaxjRO4B_dNHVtLrf8UbiM3DV2tKZhrefUQKWY2Fos130_provenance.