@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP897558.RAN5o9zVMsPtaSmR1FwYuFSptm1WkIwXryyvywuJACSYY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP897558.RAN5o9zVMsPtaSmR1FwYuFSptm1WkIwXryyvywuJACSYY130_head
{
this:
np:hasAssertion
dgn-np:NP897558.RAN5o9zVMsPtaSmR1FwYuFSptm1WkIwXryyvywuJACSYY130_assertion
;
np:hasProvenance
dgn-np:NP897558.RAN5o9zVMsPtaSmR1FwYuFSptm1WkIwXryyvywuJACSYY130_provenance
;
np:hasPublicationInfo
dgn-np:NP897558.RAN5o9zVMsPtaSmR1FwYuFSptm1WkIwXryyvywuJACSYY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP897558.RAN5o9zVMsPtaSmR1FwYuFSptm1WkIwXryyvywuJACSYY130_assertion
a
np:Assertion
.
dgn-np:NP897558.RAN5o9zVMsPtaSmR1FwYuFSptm1WkIwXryyvywuJACSYY130_provenance
a
np:Provenance
.
dgn-np:NP897558.RAN5o9zVMsPtaSmR1FwYuFSptm1WkIwXryyvywuJACSYY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP897558.RAN5o9zVMsPtaSmR1FwYuFSptm1WkIwXryyvywuJACSYY130_assertion
{
miriam-gene:340719
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGNe8cd7ea38a23ccdbee8eafc37387ee2e
sio:SIO_000628
miriam-gene:340719
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP897558.RAN5o9zVMsPtaSmR1FwYuFSptm1WkIwXryyvywuJACSYY130_provenance
{
dgn-np:NP897558.RAN5o9zVMsPtaSmR1FwYuFSptm1WkIwXryyvywuJACSYY130_assertion
dcterms:description
"[A functional variable number of tandem repeats (VNTR) polymorphism in the promoter region of the alternative first exon 1f of NOS1 is associated with various functions of human behavior, for example increased impulsivity, while another, non-functional variant was linked to decreased verbal working memory and a heightened risk for schizophrenia.]. 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:21620982
;
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:NP897558.RAN5o9zVMsPtaSmR1FwYuFSptm1WkIwXryyvywuJACSYY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:31+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}