@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_assertion
a
np:Assertion
.
dgn-np:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_provenance
a
np:Provenance
.
dgn-np:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN2894505106c5590bb53a5e3f55c5edae
sio:SIO_000628
miriam-gene:1312
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_provenance
{
dgn-np:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_assertion
dcterms:description
"[Our results will assist in the interpretation of the controversy generated by genetic associations of COMT and schizophrenia, which could be the result of different LD patterns between COMT markers and the 3' region of the ARVCF gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:19508883
;
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:NP744108.RAg9MfL7qUVnls_svzh8tpX_uZ2jUugbuVlscrrexBFcI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:22+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
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> , <
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> , <
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" .
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pav:version
"v4.0.0" .
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