@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP248302.RAkPSGZnC1AXmMEXnyUwNFAFgm4wdsH2mubEacVvMNT94
> .
@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:NP248302.RAkPSGZnC1AXmMEXnyUwNFAFgm4wdsH2mubEacVvMNT94130_head
{
this:
np:hasAssertion
dgn-np:NP248302.RAkPSGZnC1AXmMEXnyUwNFAFgm4wdsH2mubEacVvMNT94130_assertion
;
np:hasProvenance
dgn-np:NP248302.RAkPSGZnC1AXmMEXnyUwNFAFgm4wdsH2mubEacVvMNT94130_provenance
;
np:hasPublicationInfo
dgn-np:NP248302.RAkPSGZnC1AXmMEXnyUwNFAFgm4wdsH2mubEacVvMNT94130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP248302.RAkPSGZnC1AXmMEXnyUwNFAFgm4wdsH2mubEacVvMNT94130_assertion
a
np:Assertion
.
dgn-np:NP248302.RAkPSGZnC1AXmMEXnyUwNFAFgm4wdsH2mubEacVvMNT94130_provenance
a
np:Provenance
.
dgn-np:NP248302.RAkPSGZnC1AXmMEXnyUwNFAFgm4wdsH2mubEacVvMNT94130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP248302.RAkPSGZnC1AXmMEXnyUwNFAFgm4wdsH2mubEacVvMNT94130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0175697
a
ncit:C7057
.
dgn-gda:DGN6402a200e9cb18babb031727ff55aae5
sio:SIO_000628
miriam-gene:1312
,
lld:C0175697
;
a
sio:SIO_001121
.
}
dgn-np:NP248302.RAkPSGZnC1AXmMEXnyUwNFAFgm4wdsH2mubEacVvMNT94130_provenance
{
dgn-np:NP248302.RAkPSGZnC1AXmMEXnyUwNFAFgm4wdsH2mubEacVvMNT94130_assertion
dcterms:description
"[Our subjects had the same three major COMT haplotypes (termed the HPS, APS and LPS haplotypes) as previous studies have reported as regulating significantly different levels of enzymatic activity and dopamine.]. 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:20005296
;
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:NP248302.RAkPSGZnC1AXmMEXnyUwNFAFgm4wdsH2mubEacVvMNT94130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:19+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" .
}