@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP254936.RAE2Vk4eE2VJZgrydFczDOro20rczHXq0om83tWEHkdSU130_head { this: np:hasAssertion dgn-np:NP254936.RAE2Vk4eE2VJZgrydFczDOro20rczHXq0om83tWEHkdSU130_assertion; np:hasProvenance dgn-np:NP254936.RAE2Vk4eE2VJZgrydFczDOro20rczHXq0om83tWEHkdSU130_provenance; np:hasPublicationInfo dgn-np:NP254936.RAE2Vk4eE2VJZgrydFczDOro20rczHXq0om83tWEHkdSU130_publicationInfo; a np:Nanopublication . dgn-np:NP254936.RAE2Vk4eE2VJZgrydFczDOro20rczHXq0om83tWEHkdSU130_assertion a np:Assertion . dgn-np:NP254936.RAE2Vk4eE2VJZgrydFczDOro20rczHXq0om83tWEHkdSU130_provenance a np:Provenance . dgn-np:NP254936.RAE2Vk4eE2VJZgrydFczDOro20rczHXq0om83tWEHkdSU130_publicationInfo a np:PublicationInfo . } dgn-np:NP254936.RAE2Vk4eE2VJZgrydFczDOro20rczHXq0om83tWEHkdSU130_assertion { miriam-gene:3040 a ncit:C16612 . lld:C0271994 a ncit:C7057 . dgn-gda:DGN9d0c0c987e26fee20d904ea4d1a2325b sio:SIO_000628 miriam-gene:3040, lld:C0271994; a sio:SIO_001121 . } dgn-np:NP254936.RAE2Vk4eE2VJZgrydFczDOro20rczHXq0om83tWEHkdSU130_provenance { dgn-np:NP254936.RAE2Vk4eE2VJZgrydFczDOro20rczHXq0om83tWEHkdSU130_assertion dcterms:description "[The compound heterozygote is a healthy man with 43% HbF, Ggamma/Agamma ratio (27:73) differing from that of 10 simple heterozygotes for the Greek HPFH (92:8), normal levels of total Hb (13.3 g/dl), and reduced HbA2 levels comparing with the levels of beta-thal heterozygotes for the same mutation.]. 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:10367795; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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 . } dgn-np:NP254936.RAE2Vk4eE2VJZgrydFczDOro20rczHXq0om83tWEHkdSU130_publicationInfo { this: dcterms:created "2016-05-13T12:43:41+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }