@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:NP818550.RAVyCLT0IcJVMP-b13rJZA9UK9dVO5vIZVihmvnAx8Qcs130_head { this: np:hasAssertion dgn-np:NP818550.RAVyCLT0IcJVMP-b13rJZA9UK9dVO5vIZVihmvnAx8Qcs130_assertion; np:hasProvenance dgn-np:NP818550.RAVyCLT0IcJVMP-b13rJZA9UK9dVO5vIZVihmvnAx8Qcs130_provenance; np:hasPublicationInfo dgn-np:NP818550.RAVyCLT0IcJVMP-b13rJZA9UK9dVO5vIZVihmvnAx8Qcs130_publicationInfo; a np:Nanopublication . dgn-np:NP818550.RAVyCLT0IcJVMP-b13rJZA9UK9dVO5vIZVihmvnAx8Qcs130_assertion a np:Assertion . dgn-np:NP818550.RAVyCLT0IcJVMP-b13rJZA9UK9dVO5vIZVihmvnAx8Qcs130_provenance a np:Provenance . dgn-np:NP818550.RAVyCLT0IcJVMP-b13rJZA9UK9dVO5vIZVihmvnAx8Qcs130_publicationInfo a np:PublicationInfo . } dgn-np:NP818550.RAVyCLT0IcJVMP-b13rJZA9UK9dVO5vIZVihmvnAx8Qcs130_assertion { miriam-gene:3356 a ncit:C16612 . lld:C0003125 a ncit:C7057 . dgn-gda:DGN03ea0ad25f21737915da5f58d1465d60 sio:SIO_000628 miriam-gene:3356, lld:C0003125; a sio:SIO_001121 . } dgn-np:NP818550.RAVyCLT0IcJVMP-b13rJZA9UK9dVO5vIZVihmvnAx8Qcs130_provenance { dgn-np:NP818550.RAVyCLT0IcJVMP-b13rJZA9UK9dVO5vIZVihmvnAx8Qcs130_assertion dcterms:description "[Our data show a significant association between polymorphisms with the gene encoding HTR2A with both AN subtypes, an association between polymorphisms within the genes encoding HTR1D and HTR1B with RAN, and an association between polymorphisms within the gene encoding HTR2C with BPAN.]. 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:20545463; 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:NP818550.RAVyCLT0IcJVMP-b13rJZA9UK9dVO5vIZVihmvnAx8Qcs130_publicationInfo { this: dcterms:created "2016-05-13T12:47:56+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" . }