dgn-np:NP739262.RAQ2Towql8ZADY-a50dB6eKYIG1zGXxvQM9DSPoNDRPsY130_provenance {
  dgn-np:NP739262.RAQ2Towql8ZADY-a50dB6eKYIG1zGXxvQM9DSPoNDRPsY130_assertion dcterms:description "[The knowledge can be used in the following clinical settings to genotype a patient: 1) to identify a fetus at risk for hemolytic disease of the newborn 2) to genotype patients who have been recently transfused or whose erythrocytes have a positive direct antiglobulin test 3) to determine which phenotypically Fy(b-) patients have the FY*B gene, 4) to genotype when an antigen has a depressed expression on erythrocytes, 5) to mass screen for anitgen-negative donors, 6) to resolve blood group A, B, and D typing discrepancies, 7) to determine the zygosity of RhD, 8) to determine the origin of engrafted leukocytes in a stem cell recipient, 9) to determine the origin of lymphocytes in a patient with graft-versus-disease, 10) for tissue typing, 11) for paternity testing, and 12) for forensic testing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:9570701 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}