@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:NP925457.RATpmV0P2WOtOG8aTPULMNaJcSZ48DG9j4J4wPLQ4SHmM130_head { this: np:hasAssertion dgn-np:NP925457.RATpmV0P2WOtOG8aTPULMNaJcSZ48DG9j4J4wPLQ4SHmM130_assertion; np:hasProvenance dgn-np:NP925457.RATpmV0P2WOtOG8aTPULMNaJcSZ48DG9j4J4wPLQ4SHmM130_provenance; np:hasPublicationInfo dgn-np:NP925457.RATpmV0P2WOtOG8aTPULMNaJcSZ48DG9j4J4wPLQ4SHmM130_publicationInfo; a np:Nanopublication . dgn-np:NP925457.RATpmV0P2WOtOG8aTPULMNaJcSZ48DG9j4J4wPLQ4SHmM130_assertion a np:Assertion . dgn-np:NP925457.RATpmV0P2WOtOG8aTPULMNaJcSZ48DG9j4J4wPLQ4SHmM130_provenance a np:Provenance . dgn-np:NP925457.RATpmV0P2WOtOG8aTPULMNaJcSZ48DG9j4J4wPLQ4SHmM130_publicationInfo a np:PublicationInfo . } dgn-np:NP925457.RATpmV0P2WOtOG8aTPULMNaJcSZ48DG9j4J4wPLQ4SHmM130_assertion { miriam-gene:56955 a ncit:C16612 . lld:C0282193 a ncit:C7057 . dgn-gda:DGNce9c4c8425d154650a444daaa62fc718 sio:SIO_000628 miriam-gene:56955, lld:C0282193; a sio:SIO_001121 . } dgn-np:NP925457.RATpmV0P2WOtOG8aTPULMNaJcSZ48DG9j4J4wPLQ4SHmM130_provenance { dgn-np:NP925457.RATpmV0P2WOtOG8aTPULMNaJcSZ48DG9j4J4wPLQ4SHmM130_assertion dcterms:description "[Since only eight out of 45 iron-overloaded HbH patients carry a defect in the TFR2 or HFE gene in the heterozygote state and their iron loading status was comparable to the matched controls without such defects, it would appear that the accumulation of excess iron in HbH disease is more likely a result of increase dietary absorption secondary to ineffective erythropoiesis.]. 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:12667993; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP925457.RATpmV0P2WOtOG8aTPULMNaJcSZ48DG9j4J4wPLQ4SHmM130_publicationInfo { this: dcterms:created "2015-08-25T14:47:05+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }