@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP169150.RARLR5Ek_qdUDeT8PiiOIz2lURoV90ZbjACJR8XdZ13xw
> .
@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:NP169150.RARLR5Ek_qdUDeT8PiiOIz2lURoV90ZbjACJR8XdZ13xw130_head
{
this:
np:hasAssertion
dgn-np:NP169150.RARLR5Ek_qdUDeT8PiiOIz2lURoV90ZbjACJR8XdZ13xw130_assertion
;
np:hasProvenance
dgn-np:NP169150.RARLR5Ek_qdUDeT8PiiOIz2lURoV90ZbjACJR8XdZ13xw130_provenance
;
np:hasPublicationInfo
dgn-np:NP169150.RARLR5Ek_qdUDeT8PiiOIz2lURoV90ZbjACJR8XdZ13xw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP169150.RARLR5Ek_qdUDeT8PiiOIz2lURoV90ZbjACJR8XdZ13xw130_assertion
a
np:Assertion
.
dgn-np:NP169150.RARLR5Ek_qdUDeT8PiiOIz2lURoV90ZbjACJR8XdZ13xw130_provenance
a
np:Provenance
.
dgn-np:NP169150.RARLR5Ek_qdUDeT8PiiOIz2lURoV90ZbjACJR8XdZ13xw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP169150.RARLR5Ek_qdUDeT8PiiOIz2lURoV90ZbjACJR8XdZ13xw130_assertion
{
miriam-gene:1312
a
ncit:C16612
.
lld:C0476089
a
ncit:C7057
.
dgn-gda:DGN7216cb0e326ced40649748d29feaa51c
sio:SIO_000628
miriam-gene:1312
,
lld:C0476089
;
a
sio:SIO_001121
.
}
dgn-np:NP169150.RARLR5Ek_qdUDeT8PiiOIz2lURoV90ZbjACJR8XdZ13xw130_provenance
{
dgn-np:NP169150.RARLR5Ek_qdUDeT8PiiOIz2lURoV90ZbjACJR8XdZ13xw130_assertion
dcterms:description
"[This is the first study demonstrating that polymorphisms in COMT codon 62 and codon 158 altered protein expression levels in EC, suggesting that they may be risk factors for EC in Caucasians.]. 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:18324659
;
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:NP169150.RARLR5Ek_qdUDeT8PiiOIz2lURoV90ZbjACJR8XdZ13xw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:31+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: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" .
}