@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:NP440811.RA7UjyqVpBHmZKA9rA0XPZDpPIH2vG-4SXGTQu5gWw9a8130_head { this: np:hasAssertion dgn-np:NP440811.RA7UjyqVpBHmZKA9rA0XPZDpPIH2vG-4SXGTQu5gWw9a8130_assertion; np:hasProvenance dgn-np:NP440811.RA7UjyqVpBHmZKA9rA0XPZDpPIH2vG-4SXGTQu5gWw9a8130_provenance; np:hasPublicationInfo dgn-np:NP440811.RA7UjyqVpBHmZKA9rA0XPZDpPIH2vG-4SXGTQu5gWw9a8130_publicationInfo; a np:Nanopublication . dgn-np:NP440811.RA7UjyqVpBHmZKA9rA0XPZDpPIH2vG-4SXGTQu5gWw9a8130_assertion a np:Assertion . dgn-np:NP440811.RA7UjyqVpBHmZKA9rA0XPZDpPIH2vG-4SXGTQu5gWw9a8130_provenance a np:Provenance . dgn-np:NP440811.RA7UjyqVpBHmZKA9rA0XPZDpPIH2vG-4SXGTQu5gWw9a8130_publicationInfo a np:PublicationInfo . } dgn-np:NP440811.RA7UjyqVpBHmZKA9rA0XPZDpPIH2vG-4SXGTQu5gWw9a8130_assertion { miriam-gene:54808 a ncit:C16612 . lld:C0041107 a ncit:C7057 . dgn-gda:DGN14439992b75081a33d93003170ce2668 sio:SIO_000628 miriam-gene:54808, lld:C0041107; a sio:SIO_001121 . } dgn-np:NP440811.RA7UjyqVpBHmZKA9rA0XPZDpPIH2vG-4SXGTQu5gWw9a8130_provenance { dgn-np:NP440811.RA7UjyqVpBHmZKA9rA0XPZDpPIH2vG-4SXGTQu5gWw9a8130_assertion dcterms:description "[We compare the clinical characteristics of our patients with those previously reported to have either SMC including 17p or duplications of proximal 17p in an effort to further delineate the phenotype of trisomy 17p10-p11.2 and to elucidate genotype-phenotype correlations.]. 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:15098121; 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:NP440811.RA7UjyqVpBHmZKA9rA0XPZDpPIH2vG-4SXGTQu5gWw9a8130_publicationInfo { this: dcterms:created "2016-05-13T12:45:05+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" . }