@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:NP870199.RA-vXcKgNlAezMYlO9XF_6efvYrBUiHvp-TYM4MkVL5ms130_head { this: np:hasAssertion dgn-np:NP870199.RA-vXcKgNlAezMYlO9XF_6efvYrBUiHvp-TYM4MkVL5ms130_assertion; np:hasProvenance dgn-np:NP870199.RA-vXcKgNlAezMYlO9XF_6efvYrBUiHvp-TYM4MkVL5ms130_provenance; np:hasPublicationInfo dgn-np:NP870199.RA-vXcKgNlAezMYlO9XF_6efvYrBUiHvp-TYM4MkVL5ms130_publicationInfo; a np:Nanopublication . dgn-np:NP870199.RA-vXcKgNlAezMYlO9XF_6efvYrBUiHvp-TYM4MkVL5ms130_assertion a np:Assertion . dgn-np:NP870199.RA-vXcKgNlAezMYlO9XF_6efvYrBUiHvp-TYM4MkVL5ms130_provenance a np:Provenance . dgn-np:NP870199.RA-vXcKgNlAezMYlO9XF_6efvYrBUiHvp-TYM4MkVL5ms130_publicationInfo a np:PublicationInfo . } dgn-np:NP870199.RA-vXcKgNlAezMYlO9XF_6efvYrBUiHvp-TYM4MkVL5ms130_assertion { miriam-gene:23230 a ncit:C16612 . lld:C0398568 a ncit:C7057 . dgn-gda:DGN795903acdc2cd7985715c9161c03c2db sio:SIO_000628 miriam-gene:23230, lld:C0398568; a sio:SIO_001121 . } dgn-np:NP870199.RA-vXcKgNlAezMYlO9XF_6efvYrBUiHvp-TYM4MkVL5ms130_provenance { dgn-np:NP870199.RA-vXcKgNlAezMYlO9XF_6efvYrBUiHvp-TYM4MkVL5ms130_assertion dcterms:description "[We performed a comprehensive mutation screen of VPS13A and XK, the gene responsible for ChAc and MLS, respectively, in 85 mood disorder subjects and XK in 86 schizophrenia subjects and compared the variants to 100 or more control alleles.]. 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:21145924; 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:NP870199.RA-vXcKgNlAezMYlO9XF_6efvYrBUiHvp-TYM4MkVL5ms130_publicationInfo { this: dcterms:created "2015-08-25T14:46:29+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" . }