@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:NP675820.RAx7hmJCaP0tEqB76q8aqc6STDHhXZN6lRqh8KleUPF8s130_head { this: np:hasAssertion dgn-np:NP675820.RAx7hmJCaP0tEqB76q8aqc6STDHhXZN6lRqh8KleUPF8s130_assertion; np:hasProvenance dgn-np:NP675820.RAx7hmJCaP0tEqB76q8aqc6STDHhXZN6lRqh8KleUPF8s130_provenance; np:hasPublicationInfo dgn-np:NP675820.RAx7hmJCaP0tEqB76q8aqc6STDHhXZN6lRqh8KleUPF8s130_publicationInfo; a np:Nanopublication . dgn-np:NP675820.RAx7hmJCaP0tEqB76q8aqc6STDHhXZN6lRqh8KleUPF8s130_assertion a np:Assertion . dgn-np:NP675820.RAx7hmJCaP0tEqB76q8aqc6STDHhXZN6lRqh8KleUPF8s130_provenance a np:Provenance . dgn-np:NP675820.RAx7hmJCaP0tEqB76q8aqc6STDHhXZN6lRqh8KleUPF8s130_publicationInfo a np:PublicationInfo . } dgn-np:NP675820.RAx7hmJCaP0tEqB76q8aqc6STDHhXZN6lRqh8KleUPF8s130_assertion { miriam-gene:6201 a ncit:C16612 . lld:C1260899 a ncit:C7057 . dgn-gda:DGNb19675f29b9f834c54d43e2eaab98ac7 sio:SIO_000628 miriam-gene:6201, lld:C1260899; a sio:SIO_001121 . } dgn-np:NP675820.RAx7hmJCaP0tEqB76q8aqc6STDHhXZN6lRqh8KleUPF8s130_provenance { dgn-np:NP675820.RAx7hmJCaP0tEqB76q8aqc6STDHhXZN6lRqh8KleUPF8s130_assertion dcterms:description "[Recent advances in identifying the genetic abnormalities underlying DBA have demonstrated involvement of genes encoding both large (RPL) and small (RPS) ribosomal subunit proteins, including mutations of RPL5, RPL11, RPL35A, RPS7, RPS10, RPS17, RPS19, RPS24, and RPS26 in 50% to 60% of affected patients.]. 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:21435509; 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:NP675820.RAx7hmJCaP0tEqB76q8aqc6STDHhXZN6lRqh8KleUPF8s130_publicationInfo { this: dcterms:created "2015-08-25T14:44:27+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" . }