Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP130703.RAwOqIFG1OFXEwpkLNlELO0pbBL7ME2HQFOXcgTSqPP8g130_assertion> ?p ?o ?g. }
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- NP130703.RAwOqIFG1OFXEwpkLNlELO0pbBL7ME2HQFOXcgTSqPP8g130_assertion type Assertion NP130703.RAwOqIFG1OFXEwpkLNlELO0pbBL7ME2HQFOXcgTSqPP8g130_head.
- NP130703.RAwOqIFG1OFXEwpkLNlELO0pbBL7ME2HQFOXcgTSqPP8g130_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." NP130703.RAwOqIFG1OFXEwpkLNlELO0pbBL7ME2HQFOXcgTSqPP8g130_provenance.
- NP130703.RAwOqIFG1OFXEwpkLNlELO0pbBL7ME2HQFOXcgTSqPP8g130_assertion evidence source_evidence_literature NP130703.RAwOqIFG1OFXEwpkLNlELO0pbBL7ME2HQFOXcgTSqPP8g130_provenance.
- NP130703.RAwOqIFG1OFXEwpkLNlELO0pbBL7ME2HQFOXcgTSqPP8g130_assertion SIO_000772 18264947 NP130703.RAwOqIFG1OFXEwpkLNlELO0pbBL7ME2HQFOXcgTSqPP8g130_provenance.
- NP130703.RAwOqIFG1OFXEwpkLNlELO0pbBL7ME2HQFOXcgTSqPP8g130_assertion wasDerivedFrom gad-20150221 NP130703.RAwOqIFG1OFXEwpkLNlELO0pbBL7ME2HQFOXcgTSqPP8g130_provenance.
- NP130703.RAwOqIFG1OFXEwpkLNlELO0pbBL7ME2HQFOXcgTSqPP8g130_assertion wasGeneratedBy ECO_0000203 NP130703.RAwOqIFG1OFXEwpkLNlELO0pbBL7ME2HQFOXcgTSqPP8g130_provenance.