@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:NP960807.RAr7ZaUddDAvmD5VIGYajrC3LOofGcdB7EkNWzd-Nwmas130_head { this: np:hasAssertion dgn-np:NP960807.RAr7ZaUddDAvmD5VIGYajrC3LOofGcdB7EkNWzd-Nwmas130_assertion; np:hasProvenance dgn-np:NP960807.RAr7ZaUddDAvmD5VIGYajrC3LOofGcdB7EkNWzd-Nwmas130_provenance; np:hasPublicationInfo dgn-np:NP960807.RAr7ZaUddDAvmD5VIGYajrC3LOofGcdB7EkNWzd-Nwmas130_publicationInfo; a np:Nanopublication . dgn-np:NP960807.RAr7ZaUddDAvmD5VIGYajrC3LOofGcdB7EkNWzd-Nwmas130_assertion a np:Assertion . dgn-np:NP960807.RAr7ZaUddDAvmD5VIGYajrC3LOofGcdB7EkNWzd-Nwmas130_provenance a np:Provenance . dgn-np:NP960807.RAr7ZaUddDAvmD5VIGYajrC3LOofGcdB7EkNWzd-Nwmas130_publicationInfo a np:PublicationInfo . } dgn-np:NP960807.RAr7ZaUddDAvmD5VIGYajrC3LOofGcdB7EkNWzd-Nwmas130_assertion { miriam-gene:91452 a ncit:C16612 . lld:C0854723 a ncit:C7057 . dgn-gda:DGNd081f5bc85b09a9918b0092a7868b556 sio:SIO_000628 miriam-gene:91452, lld:C0854723; a sio:SIO_001121 . } dgn-np:NP960807.RAr7ZaUddDAvmD5VIGYajrC3LOofGcdB7EkNWzd-Nwmas130_provenance { dgn-np:NP960807.RAr7ZaUddDAvmD5VIGYajrC3LOofGcdB7EkNWzd-Nwmas130_assertion dcterms:description "[Additionally, our study revealed six novel candidate disease genes (C21orf2, EMC1, KIAA1549, GPR125, ACBD5, and DTHD1), two of which (ACBD5 and DTHD1) were observed in the context of syndromic forms of RD that are described for the first time.]. 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:23105016; 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:NP960807.RAr7ZaUddDAvmD5VIGYajrC3LOofGcdB7EkNWzd-Nwmas130_publicationInfo { this: dcterms:created "2015-08-25T14:47:26+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" . }