Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP84262.RALVo0aQAlUE-1ArQMVhkymeGp3fUoc-acuHr_RT5KZlI130_assertion> ?p ?o ?g. }
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- NP84262.RALVo0aQAlUE-1ArQMVhkymeGp3fUoc-acuHr_RT5KZlI130_assertion type Assertion NP84262.RALVo0aQAlUE-1ArQMVhkymeGp3fUoc-acuHr_RT5KZlI130_head.
- NP84262.RALVo0aQAlUE-1ArQMVhkymeGp3fUoc-acuHr_RT5KZlI130_assertion description "[Carrier frequency of autosomal-recessive disorders in the Ashkenazi Jewish population: should the rationale for mutation choice for screening be reevaluated?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP84262.RALVo0aQAlUE-1ArQMVhkymeGp3fUoc-acuHr_RT5KZlI130_provenance.
- NP84262.RALVo0aQAlUE-1ArQMVhkymeGp3fUoc-acuHr_RT5KZlI130_assertion evidence source_evidence_literature NP84262.RALVo0aQAlUE-1ArQMVhkymeGp3fUoc-acuHr_RT5KZlI130_provenance.
- NP84262.RALVo0aQAlUE-1ArQMVhkymeGp3fUoc-acuHr_RT5KZlI130_assertion SIO_000772 18264947 NP84262.RALVo0aQAlUE-1ArQMVhkymeGp3fUoc-acuHr_RT5KZlI130_provenance.
- NP84262.RALVo0aQAlUE-1ArQMVhkymeGp3fUoc-acuHr_RT5KZlI130_assertion wasDerivedFrom gad-20130706 NP84262.RALVo0aQAlUE-1ArQMVhkymeGp3fUoc-acuHr_RT5KZlI130_provenance.
- NP84262.RALVo0aQAlUE-1ArQMVhkymeGp3fUoc-acuHr_RT5KZlI130_assertion wasGeneratedBy ECO_0000203 NP84262.RALVo0aQAlUE-1ArQMVhkymeGp3fUoc-acuHr_RT5KZlI130_provenance.