@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:NP633866.RAQxVTLqCuOTrYQLzEXre6_iCKEaXRrblkwuHbH3qtLAA130_head { this: np:hasAssertion dgn-np:NP633866.RAQxVTLqCuOTrYQLzEXre6_iCKEaXRrblkwuHbH3qtLAA130_assertion; np:hasProvenance dgn-np:NP633866.RAQxVTLqCuOTrYQLzEXre6_iCKEaXRrblkwuHbH3qtLAA130_provenance; np:hasPublicationInfo dgn-np:NP633866.RAQxVTLqCuOTrYQLzEXre6_iCKEaXRrblkwuHbH3qtLAA130_publicationInfo; a np:Nanopublication . dgn-np:NP633866.RAQxVTLqCuOTrYQLzEXre6_iCKEaXRrblkwuHbH3qtLAA130_assertion a np:Assertion . dgn-np:NP633866.RAQxVTLqCuOTrYQLzEXre6_iCKEaXRrblkwuHbH3qtLAA130_provenance a np:Provenance . dgn-np:NP633866.RAQxVTLqCuOTrYQLzEXre6_iCKEaXRrblkwuHbH3qtLAA130_publicationInfo a np:PublicationInfo . } dgn-np:NP633866.RAQxVTLqCuOTrYQLzEXre6_iCKEaXRrblkwuHbH3qtLAA130_assertion { miriam-gene:3043 a ncit:C16612 . lld:C0002895 a ncit:C7057 . dgn-gda:DGNbf1ba9d4e841329fdd78359e6ee618c2 sio:SIO_000628 miriam-gene:3043, lld:C0002895; a sio:SIO_001121 . } dgn-np:NP633866.RAQxVTLqCuOTrYQLzEXre6_iCKEaXRrblkwuHbH3qtLAA130_provenance { dgn-np:NP633866.RAQxVTLqCuOTrYQLzEXre6_iCKEaXRrblkwuHbH3qtLAA130_assertion dcterms:description "[We genotyped single nucleotide polymorphisms (SNPs) in: (1) the beta-globin gene-like cluster, (2) quantitative trait loci (QTL) previously associated with fetal hemoglobin (HbF) concentration on chromosomes 6q, 8q, and Xp, and (3) candidate genes that could effect HbF levels, in sickle cell anemia subjects.]. 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:17918249; 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:NP633866.RAQxVTLqCuOTrYQLzEXre6_iCKEaXRrblkwuHbH3qtLAA130_publicationInfo { this: dcterms:created "2016-05-13T12:46:33+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" . }