Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP93014.RA-Qo0wINJYer7WUYF-ANQLBZ46zs1pTo3ch-JbTk--CU130_assertion> ?p ?o ?g. }
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- NP93014.RA-Qo0wINJYer7WUYF-ANQLBZ46zs1pTo3ch-JbTk--CU130_assertion type Assertion NP93014.RA-Qo0wINJYer7WUYF-ANQLBZ46zs1pTo3ch-JbTk--CU130_head.
- NP93014.RA-Qo0wINJYer7WUYF-ANQLBZ46zs1pTo3ch-JbTk--CU130_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." NP93014.RA-Qo0wINJYer7WUYF-ANQLBZ46zs1pTo3ch-JbTk--CU130_provenance.
- NP93014.RA-Qo0wINJYer7WUYF-ANQLBZ46zs1pTo3ch-JbTk--CU130_assertion evidence source_evidence_literature NP93014.RA-Qo0wINJYer7WUYF-ANQLBZ46zs1pTo3ch-JbTk--CU130_provenance.
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- NP93014.RA-Qo0wINJYer7WUYF-ANQLBZ46zs1pTo3ch-JbTk--CU130_assertion wasDerivedFrom gad-20130706 NP93014.RA-Qo0wINJYer7WUYF-ANQLBZ46zs1pTo3ch-JbTk--CU130_provenance.
- NP93014.RA-Qo0wINJYer7WUYF-ANQLBZ46zs1pTo3ch-JbTk--CU130_assertion wasGeneratedBy ECO_0000203 NP93014.RA-Qo0wINJYer7WUYF-ANQLBZ46zs1pTo3ch-JbTk--CU130_provenance.