@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:NP1309707.RAsjTtJ1pnlr2swYcowvJNP9UJUk6g0XSPMRTbGhhu-dU130_head { this: np:hasAssertion dgn-np:NP1309707.RAsjTtJ1pnlr2swYcowvJNP9UJUk6g0XSPMRTbGhhu-dU130_assertion; np:hasProvenance dgn-np:NP1309707.RAsjTtJ1pnlr2swYcowvJNP9UJUk6g0XSPMRTbGhhu-dU130_provenance; np:hasPublicationInfo dgn-np:NP1309707.RAsjTtJ1pnlr2swYcowvJNP9UJUk6g0XSPMRTbGhhu-dU130_publicationInfo; a np:Nanopublication . dgn-np:NP1309707.RAsjTtJ1pnlr2swYcowvJNP9UJUk6g0XSPMRTbGhhu-dU130_assertion a np:Assertion . dgn-np:NP1309707.RAsjTtJ1pnlr2swYcowvJNP9UJUk6g0XSPMRTbGhhu-dU130_provenance a np:Provenance . dgn-np:NP1309707.RAsjTtJ1pnlr2swYcowvJNP9UJUk6g0XSPMRTbGhhu-dU130_publicationInfo a np:PublicationInfo . } dgn-np:NP1309707.RAsjTtJ1pnlr2swYcowvJNP9UJUk6g0XSPMRTbGhhu-dU130_assertion { miriam-gene:1154 a ncit:C16612 . lld:C0221228 a ncit:C7057 . dgn-gda:DGN57e56e757913b240121e43979130e97e sio:SIO_000628 miriam-gene:1154, lld:C0221228; a sio:SIO_001121 . } dgn-np:NP1309707.RAsjTtJ1pnlr2swYcowvJNP9UJUk6g0XSPMRTbGhhu-dU130_provenance { dgn-np:NP1309707.RAsjTtJ1pnlr2swYcowvJNP9UJUk6g0XSPMRTbGhhu-dU130_assertion dcterms:description "[Comparing subtypes of CIS in the groups with or without invasion, only comedo DCIS was significantly different, with greater expression in the CIS group with no invasion compared with comedo DCIS associated with an invasive component (P = 0.04).]. 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:7513249; 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:NP1309707.RAsjTtJ1pnlr2swYcowvJNP9UJUk6g0XSPMRTbGhhu-dU130_publicationInfo { this: dcterms:created "2016-05-13T12:51:39+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" . }