@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:NP978802.RAh_I-EfMosY4m0qC_QdgJgJ0dY8Oz2p0ci1C31LYZKQI130_head { this: np:hasAssertion dgn-np:NP978802.RAh_I-EfMosY4m0qC_QdgJgJ0dY8Oz2p0ci1C31LYZKQI130_assertion; np:hasProvenance dgn-np:NP978802.RAh_I-EfMosY4m0qC_QdgJgJ0dY8Oz2p0ci1C31LYZKQI130_provenance; np:hasPublicationInfo dgn-np:NP978802.RAh_I-EfMosY4m0qC_QdgJgJ0dY8Oz2p0ci1C31LYZKQI130_publicationInfo; a np:Nanopublication . dgn-np:NP978802.RAh_I-EfMosY4m0qC_QdgJgJ0dY8Oz2p0ci1C31LYZKQI130_assertion a np:Assertion . dgn-np:NP978802.RAh_I-EfMosY4m0qC_QdgJgJ0dY8Oz2p0ci1C31LYZKQI130_provenance a np:Provenance . dgn-np:NP978802.RAh_I-EfMosY4m0qC_QdgJgJ0dY8Oz2p0ci1C31LYZKQI130_publicationInfo a np:PublicationInfo . } dgn-np:NP978802.RAh_I-EfMosY4m0qC_QdgJgJ0dY8Oz2p0ci1C31LYZKQI130_assertion { miriam-gene:191585 a ncit:C16612 . lld:C0013080 a ncit:C7057 . dgn-gda:DGNbb814ddfd4dc706b1609b895bfbe71a2 sio:SIO_000628 miriam-gene:191585, lld:C0013080; a sio:SIO_001121 . } dgn-np:NP978802.RAh_I-EfMosY4m0qC_QdgJgJ0dY8Oz2p0ci1C31LYZKQI130_provenance { dgn-np:NP978802.RAh_I-EfMosY4m0qC_QdgJgJ0dY8Oz2p0ci1C31LYZKQI130_assertion dcterms:description "[We achieved noninvasive prenatal diagnosis of fetal trisomy 21 by determining the ratio between alleles of a single-nucleotide polymorphism (SNP) in PLAC4 mRNA, which is transcribed from chromosome 21 and expressed by the placenta, in maternal plasma.]. 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:17206148; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP978802.RAh_I-EfMosY4m0qC_QdgJgJ0dY8Oz2p0ci1C31LYZKQI130_publicationInfo { this: dcterms:created "2015-08-25T14:47:38+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }