@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:NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_head { this: np:hasAssertion dgn-np:NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_assertion; np:hasProvenance dgn-np:NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_provenance; np:hasPublicationInfo dgn-np:NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_publicationInfo; a np:Nanopublication . dgn-np:NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_assertion a np:Assertion . dgn-np:NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_provenance a np:Provenance . dgn-np:NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_publicationInfo a np:PublicationInfo . } dgn-np:NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_assertion { miriam-gene:8710 a ncit:C16612 . lld:C0022661 a ncit:C7057 . dgn-gda:DGNe2e3d88d7a3a168bb5e26a642378f343 sio:SIO_000628 miriam-gene:8710, lld:C0022661; a sio:SIO_001122 . } dgn-np:NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_provenance { dgn-np:NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_assertion dcterms:description "[We investigated a possible association of two C2093T, C2180T polymorphisms of the megsin gene with the progression of IgAN towards ESRD, as well as the haplotype reconstruction of megsin gene polymorphisms and clinical manifestation of IgAN.]. 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:18498720; 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:NP672739.RAbh-_dh60bakNbZFzeMt4NlcSzE1dcv7zgfX8_TOQM3w130_publicationInfo { this: dcterms:created "2016-05-13T12:46:50+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" . }