Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP86683.RA_bGM6Du2YO8_UWa1DhUYPtfFm1SHMCN14T2rcUVcIaA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP86683.RA_bGM6Du2YO8_UWa1DhUYPtfFm1SHMCN14T2rcUVcIaA130_assertion type Assertion NP86683.RA_bGM6Du2YO8_UWa1DhUYPtfFm1SHMCN14T2rcUVcIaA130_head.
- NP86683.RA_bGM6Du2YO8_UWa1DhUYPtfFm1SHMCN14T2rcUVcIaA130_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." NP86683.RA_bGM6Du2YO8_UWa1DhUYPtfFm1SHMCN14T2rcUVcIaA130_provenance.
- NP86683.RA_bGM6Du2YO8_UWa1DhUYPtfFm1SHMCN14T2rcUVcIaA130_assertion evidence source_evidence_literature NP86683.RA_bGM6Du2YO8_UWa1DhUYPtfFm1SHMCN14T2rcUVcIaA130_provenance.
- NP86683.RA_bGM6Du2YO8_UWa1DhUYPtfFm1SHMCN14T2rcUVcIaA130_assertion SIO_000772 18264947 NP86683.RA_bGM6Du2YO8_UWa1DhUYPtfFm1SHMCN14T2rcUVcIaA130_provenance.
- NP86683.RA_bGM6Du2YO8_UWa1DhUYPtfFm1SHMCN14T2rcUVcIaA130_assertion wasDerivedFrom gad-20130706 NP86683.RA_bGM6Du2YO8_UWa1DhUYPtfFm1SHMCN14T2rcUVcIaA130_provenance.
- NP86683.RA_bGM6Du2YO8_UWa1DhUYPtfFm1SHMCN14T2rcUVcIaA130_assertion wasGeneratedBy ECO_0000203 NP86683.RA_bGM6Du2YO8_UWa1DhUYPtfFm1SHMCN14T2rcUVcIaA130_provenance.