@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:NP964316.RA_3LHmWFScdOt6lJBlkS4EGTowpbtx_e8aBE4wboa6lU130_head { this: np:hasAssertion dgn-np:NP964316.RA_3LHmWFScdOt6lJBlkS4EGTowpbtx_e8aBE4wboa6lU130_assertion; np:hasProvenance dgn-np:NP964316.RA_3LHmWFScdOt6lJBlkS4EGTowpbtx_e8aBE4wboa6lU130_provenance; np:hasPublicationInfo dgn-np:NP964316.RA_3LHmWFScdOt6lJBlkS4EGTowpbtx_e8aBE4wboa6lU130_publicationInfo; a np:Nanopublication . dgn-np:NP964316.RA_3LHmWFScdOt6lJBlkS4EGTowpbtx_e8aBE4wboa6lU130_assertion a np:Assertion . dgn-np:NP964316.RA_3LHmWFScdOt6lJBlkS4EGTowpbtx_e8aBE4wboa6lU130_provenance a np:Provenance . dgn-np:NP964316.RA_3LHmWFScdOt6lJBlkS4EGTowpbtx_e8aBE4wboa6lU130_publicationInfo a np:PublicationInfo . } dgn-np:NP964316.RA_3LHmWFScdOt6lJBlkS4EGTowpbtx_e8aBE4wboa6lU130_assertion { miriam-gene:114086 a ncit:C16612 . lld:C1260899 a ncit:C7057 . dgn-gda:DGNe2f3c872d4f9ac1ff715a788c10a5f74 sio:SIO_000628 miriam-gene:114086, lld:C1260899; a sio:SIO_001122 . } dgn-np:NP964316.RA_3LHmWFScdOt6lJBlkS4EGTowpbtx_e8aBE4wboa6lU130_provenance { dgn-np:NP964316.RA_3LHmWFScdOt6lJBlkS4EGTowpbtx_e8aBE4wboa6lU130_assertion dcterms:description "[Furthermore, we determined that the D2.B6N-Asp1b mouse expresses both the D2 phenotype and genotype at the Ahr locus, i.e., zoxazolamine paralysis and T to C and G to A transition mutations in the Ahr cDNA at bp sites 3330 and 3336, respectively.]. 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:10656108; 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:NP964316.RA_3LHmWFScdOt6lJBlkS4EGTowpbtx_e8aBE4wboa6lU130_publicationInfo { this: dcterms:created "2015-08-25T14:47:29+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" . }