@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:NP283034.RABSxPP_l5rw_-I-N6K8FZz4VknQoG_YgBeHnLmw9KY4Y130_head { this: np:hasAssertion dgn-np:NP283034.RABSxPP_l5rw_-I-N6K8FZz4VknQoG_YgBeHnLmw9KY4Y130_assertion; np:hasProvenance dgn-np:NP283034.RABSxPP_l5rw_-I-N6K8FZz4VknQoG_YgBeHnLmw9KY4Y130_provenance; np:hasPublicationInfo dgn-np:NP283034.RABSxPP_l5rw_-I-N6K8FZz4VknQoG_YgBeHnLmw9KY4Y130_publicationInfo; a np:Nanopublication . dgn-np:NP283034.RABSxPP_l5rw_-I-N6K8FZz4VknQoG_YgBeHnLmw9KY4Y130_assertion a np:Assertion . dgn-np:NP283034.RABSxPP_l5rw_-I-N6K8FZz4VknQoG_YgBeHnLmw9KY4Y130_provenance a np:Provenance . dgn-np:NP283034.RABSxPP_l5rw_-I-N6K8FZz4VknQoG_YgBeHnLmw9KY4Y130_publicationInfo a np:PublicationInfo . } dgn-np:NP283034.RABSxPP_l5rw_-I-N6K8FZz4VknQoG_YgBeHnLmw9KY4Y130_assertion { miriam-gene:4316 a ncit:C16612 . lld:C0027627 a ncit:C7057 . dgn-gda:DGN3a43c4c1c194a70dada1e5f036c44a3e sio:SIO_000628 miriam-gene:4316, lld:C0027627; a sio:SIO_001121 . } dgn-np:NP283034.RABSxPP_l5rw_-I-N6K8FZz4VknQoG_YgBeHnLmw9KY4Y130_provenance { dgn-np:NP283034.RABSxPP_l5rw_-I-N6K8FZz4VknQoG_YgBeHnLmw9KY4Y130_assertion dcterms:description "[The results showed that: (1) The genotype frequency of IL-8 -251AT and TT was significantly higher in the cervical cancer group than in the normal control group (OR=2.290 and 2.619 respectively, P=0.001), and it was also higher in the lymphatic metastasis group than that without metastasis (OR=2.917, P=0.035); (2) The frequency of MMP-7 -181G/G genotype was significantly higher in the cervical cancer group and in the lymphatic metastasis group (P<0.05); (3) The incidence of IL-8 mutation was two times higher in IIa cervical cancer group than in Ib1 and Ib2 cervical cancer group (P=0.006).]. 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:21336735; prov:wasDerivedFrom dgn-void:befree-20140225; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP283034.RABSxPP_l5rw_-I-N6K8FZz4VknQoG_YgBeHnLmw9KY4Y130_publicationInfo { this: dcterms:created "2014-10-02T12:34:39+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetrdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v2.1.0.0" . dgn-void:disgenetrdf pav:version "v2.1.0" . }