@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:NP1105830.RALd3DnT_gb98iIrGbBNAO0Vg2Ku7e9zo4zMFZIAqWzII130_head { this: np:hasAssertion dgn-np:NP1105830.RALd3DnT_gb98iIrGbBNAO0Vg2Ku7e9zo4zMFZIAqWzII130_assertion; np:hasProvenance dgn-np:NP1105830.RALd3DnT_gb98iIrGbBNAO0Vg2Ku7e9zo4zMFZIAqWzII130_provenance; np:hasPublicationInfo dgn-np:NP1105830.RALd3DnT_gb98iIrGbBNAO0Vg2Ku7e9zo4zMFZIAqWzII130_publicationInfo; a np:Nanopublication . dgn-np:NP1105830.RALd3DnT_gb98iIrGbBNAO0Vg2Ku7e9zo4zMFZIAqWzII130_assertion a np:Assertion . dgn-np:NP1105830.RALd3DnT_gb98iIrGbBNAO0Vg2Ku7e9zo4zMFZIAqWzII130_provenance a np:Provenance . dgn-np:NP1105830.RALd3DnT_gb98iIrGbBNAO0Vg2Ku7e9zo4zMFZIAqWzII130_publicationInfo a np:PublicationInfo . } dgn-np:NP1105830.RALd3DnT_gb98iIrGbBNAO0Vg2Ku7e9zo4zMFZIAqWzII130_assertion { miriam-gene:51196 a ncit:C16612 . lld:C0279626 a ncit:C7057 . dgn-gda:DGNcc88588e58b14e0dfdae03d8820ac26c sio:SIO_000628 miriam-gene:51196, lld:C0279626; a sio:SIO_001121 . } dgn-np:NP1105830.RALd3DnT_gb98iIrGbBNAO0Vg2Ku7e9zo4zMFZIAqWzII130_provenance { dgn-np:NP1105830.RALd3DnT_gb98iIrGbBNAO0Vg2Ku7e9zo4zMFZIAqWzII130_assertion dcterms:description "[Our findings suggested that genetic variants in PLCE1 might serve as candidate markers for Kazakh ESCC susceptibility, and these LD variants might influence ESCC risk individually and jointly by promoting the messenger RNA and protein expression of the gene.]. 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:23981775; 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:NP1105830.RALd3DnT_gb98iIrGbBNAO0Vg2Ku7e9zo4zMFZIAqWzII130_publicationInfo { this: dcterms:created "2016-05-13T12:50:07+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" . }