@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:NP816947.RA-TpnfO4n83U_ZZua7HjlqEEIqOPumYQ69laEDlBVulY130_head { this: np:hasAssertion dgn-np:NP816947.RA-TpnfO4n83U_ZZua7HjlqEEIqOPumYQ69laEDlBVulY130_assertion; np:hasProvenance dgn-np:NP816947.RA-TpnfO4n83U_ZZua7HjlqEEIqOPumYQ69laEDlBVulY130_provenance; np:hasPublicationInfo dgn-np:NP816947.RA-TpnfO4n83U_ZZua7HjlqEEIqOPumYQ69laEDlBVulY130_publicationInfo; a np:Nanopublication . dgn-np:NP816947.RA-TpnfO4n83U_ZZua7HjlqEEIqOPumYQ69laEDlBVulY130_assertion a np:Assertion . dgn-np:NP816947.RA-TpnfO4n83U_ZZua7HjlqEEIqOPumYQ69laEDlBVulY130_provenance a np:Provenance . dgn-np:NP816947.RA-TpnfO4n83U_ZZua7HjlqEEIqOPumYQ69laEDlBVulY130_publicationInfo a np:PublicationInfo . } dgn-np:NP816947.RA-TpnfO4n83U_ZZua7HjlqEEIqOPumYQ69laEDlBVulY130_assertion { miriam-gene:9173 a ncit:C16612 . lld:C1956097 a ncit:C7057 . dgn-gda:DGN6d01ce5a34b3ff49f6b4a80660b31212 sio:SIO_000628 miriam-gene:9173, lld:C1956097; a sio:SIO_001122 . } dgn-np:NP816947.RA-TpnfO4n83U_ZZua7HjlqEEIqOPumYQ69laEDlBVulY130_provenance { dgn-np:NP816947.RA-TpnfO4n83U_ZZua7HjlqEEIqOPumYQ69laEDlBVulY130_assertion dcterms:description "[Among the 103 traits identified in the child with unbalanced translocation der(4)t(4;11)(p16.1;q23.3), most clinical and developmental traits (but only 11 morphological) were found to be shared by WHS children with pure M4p16.1 and at least one reported patient with pure 11q trisomy.]. 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:21744486; 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:NP816947.RA-TpnfO4n83U_ZZua7HjlqEEIqOPumYQ69laEDlBVulY130_publicationInfo { this: dcterms:created "2015-08-25T14:45:55+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" . }