@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP657276.RALTO4RB_NWvO88oK9XSxETuCXfUV5PZp7QVA60KlPfHE
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP657276.RALTO4RB_NWvO88oK9XSxETuCXfUV5PZp7QVA60KlPfHE130_head
{
this:
np:hasAssertion
dgn-np:NP657276.RALTO4RB_NWvO88oK9XSxETuCXfUV5PZp7QVA60KlPfHE130_assertion
;
np:hasProvenance
dgn-np:NP657276.RALTO4RB_NWvO88oK9XSxETuCXfUV5PZp7QVA60KlPfHE130_provenance
;
np:hasPublicationInfo
dgn-np:NP657276.RALTO4RB_NWvO88oK9XSxETuCXfUV5PZp7QVA60KlPfHE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP657276.RALTO4RB_NWvO88oK9XSxETuCXfUV5PZp7QVA60KlPfHE130_assertion
a
np:Assertion
.
dgn-np:NP657276.RALTO4RB_NWvO88oK9XSxETuCXfUV5PZp7QVA60KlPfHE130_provenance
a
np:Provenance
.
dgn-np:NP657276.RALTO4RB_NWvO88oK9XSxETuCXfUV5PZp7QVA60KlPfHE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP657276.RALTO4RB_NWvO88oK9XSxETuCXfUV5PZp7QVA60KlPfHE130_assertion
{
miriam-gene:6899
a
ncit:C16612
.
lld:C0004936
a
ncit:C7057
.
dgn-gda:DGN0a8c4217d14173ab3f93f4297e24b66a
sio:SIO_000628
miriam-gene:6899
,
lld:C0004936
;
a
sio:SIO_001121
.
}
dgn-np:NP657276.RALTO4RB_NWvO88oK9XSxETuCXfUV5PZp7QVA60KlPfHE130_provenance
{
dgn-np:NP657276.RALTO4RB_NWvO88oK9XSxETuCXfUV5PZp7QVA60KlPfHE130_assertion
dcterms:description
"[Individuals with VCFS present with deficits in cognition and social functioning, high risk of psychiatric disorders, volumetric reductions in gray and white matter (WM) and some alterations of the WM microstructure.]. 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:22853778
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP657276.RALTO4RB_NWvO88oK9XSxETuCXfUV5PZp7QVA60KlPfHE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:35+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}