@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:NP90851.RA4hZuWgW0y_DvgiNeYoepQefpFwSf7zyP_WW3T41wl98130_head { this: np:hasAssertion dgn-np:NP90851.RA4hZuWgW0y_DvgiNeYoepQefpFwSf7zyP_WW3T41wl98130_assertion; np:hasProvenance dgn-np:NP90851.RA4hZuWgW0y_DvgiNeYoepQefpFwSf7zyP_WW3T41wl98130_provenance; np:hasPublicationInfo dgn-np:NP90851.RA4hZuWgW0y_DvgiNeYoepQefpFwSf7zyP_WW3T41wl98130_publicationInfo; a np:Nanopublication . dgn-np:NP90851.RA4hZuWgW0y_DvgiNeYoepQefpFwSf7zyP_WW3T41wl98130_assertion a np:Assertion . dgn-np:NP90851.RA4hZuWgW0y_DvgiNeYoepQefpFwSf7zyP_WW3T41wl98130_provenance a np:Provenance . dgn-np:NP90851.RA4hZuWgW0y_DvgiNeYoepQefpFwSf7zyP_WW3T41wl98130_publicationInfo a np:PublicationInfo . } dgn-np:NP90851.RA4hZuWgW0y_DvgiNeYoepQefpFwSf7zyP_WW3T41wl98130_assertion { miriam-gene:3690 a ncit:C16612 . lld:C0333186 a ncit:C7057 . dgn-gda:DGN4a34f00a3443ad16e9645d46c9625e18 sio:SIO_000628 miriam-gene:3690, lld:C0333186; a sio:SIO_001122 . } dgn-np:NP90851.RA4hZuWgW0y_DvgiNeYoepQefpFwSf7zyP_WW3T41wl98130_provenance { dgn-np:NP90851.RA4hZuWgW0y_DvgiNeYoepQefpFwSf7zyP_WW3T41wl98130_assertion dcterms:description "[This study is of great importance (i) particularly in the context of the diversity caused by the population migrations, we may observe today in our hospitals (ii) to confirm that the Pygmy population with distinctive frequencies (absence of the HPA-1b, HP]. 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:15730528; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP90851.RA4hZuWgW0y_DvgiNeYoepQefpFwSf7zyP_WW3T41wl98130_publicationInfo { this: dcterms:created "2016-05-13T12:42:29+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" . }