@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:NP1208131.RAgalS3167eE8x9aJA0no1GXguD2TMcBDfzf46NB7J7n8130_head { this: np:hasAssertion dgn-np:NP1208131.RAgalS3167eE8x9aJA0no1GXguD2TMcBDfzf46NB7J7n8130_assertion; np:hasProvenance dgn-np:NP1208131.RAgalS3167eE8x9aJA0no1GXguD2TMcBDfzf46NB7J7n8130_provenance; np:hasPublicationInfo dgn-np:NP1208131.RAgalS3167eE8x9aJA0no1GXguD2TMcBDfzf46NB7J7n8130_publicationInfo; a np:Nanopublication . dgn-np:NP1208131.RAgalS3167eE8x9aJA0no1GXguD2TMcBDfzf46NB7J7n8130_assertion a np:Assertion . dgn-np:NP1208131.RAgalS3167eE8x9aJA0no1GXguD2TMcBDfzf46NB7J7n8130_provenance a np:Provenance . dgn-np:NP1208131.RAgalS3167eE8x9aJA0no1GXguD2TMcBDfzf46NB7J7n8130_publicationInfo a np:PublicationInfo . } dgn-np:NP1208131.RAgalS3167eE8x9aJA0no1GXguD2TMcBDfzf46NB7J7n8130_assertion { miriam-gene:199713 a ncit:C16612 . lld:C0020217 a ncit:C7057 . dgn-gda:DGN54c8f91ee90bc568e34acde5dd579720 sio:SIO_000628 miriam-gene:199713, lld:C0020217; a sio:SIO_001121 . } dgn-np:NP1208131.RAgalS3167eE8x9aJA0no1GXguD2TMcBDfzf46NB7J7n8130_provenance { dgn-np:NP1208131.RAgalS3167eE8x9aJA0no1GXguD2TMcBDfzf46NB7J7n8130_assertion dcterms:description "[In this study, we characterised the expression of the imprinted, maternally expressed gene, CDKN1C (p57(KIP2)), the genotype, and the histopathology of 36 products of conception (POC) from patients with two defective alleles in NLRP7 and looked for potential correlations between the nature of the mutations in the patients and the various HM features.]. 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:25097207; 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:NP1208131.RAgalS3167eE8x9aJA0no1GXguD2TMcBDfzf46NB7J7n8130_publicationInfo { this: dcterms:created "2016-05-13T12:50:53+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" . }