@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP721168.RA7qBLkULtrr7ckVO8foIiaSK6mZoHpGEKip15brA_Na4
> .
@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:NP721168.RA7qBLkULtrr7ckVO8foIiaSK6mZoHpGEKip15brA_Na4130_head
{
this:
np:hasAssertion
dgn-np:NP721168.RA7qBLkULtrr7ckVO8foIiaSK6mZoHpGEKip15brA_Na4130_assertion
;
np:hasProvenance
dgn-np:NP721168.RA7qBLkULtrr7ckVO8foIiaSK6mZoHpGEKip15brA_Na4130_provenance
;
np:hasPublicationInfo
dgn-np:NP721168.RA7qBLkULtrr7ckVO8foIiaSK6mZoHpGEKip15brA_Na4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP721168.RA7qBLkULtrr7ckVO8foIiaSK6mZoHpGEKip15brA_Na4130_assertion
a
np:Assertion
.
dgn-np:NP721168.RA7qBLkULtrr7ckVO8foIiaSK6mZoHpGEKip15brA_Na4130_provenance
a
np:Provenance
.
dgn-np:NP721168.RA7qBLkULtrr7ckVO8foIiaSK6mZoHpGEKip15brA_Na4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP721168.RA7qBLkULtrr7ckVO8foIiaSK6mZoHpGEKip15brA_Na4130_assertion
{
miriam-gene:2100
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNaeb02836e4bc024df70ba8d44ba5b268
sio:SIO_000628
miriam-gene:2100
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP721168.RA7qBLkULtrr7ckVO8foIiaSK6mZoHpGEKip15brA_Na4130_provenance
{
dgn-np:NP721168.RA7qBLkULtrr7ckVO8foIiaSK6mZoHpGEKip15brA_Na4130_assertion
dcterms:description
"[The observed increased risk of PD among female but not male carriers of the rs762551 polymorphism of CYP1A2 and the interactions of caffeine with ESR1 rs3798577 and ESR2 rs1255998 may provide clues to explain the relationship between gender, caffeine intake, estrogen status and risk of PD and need to be replicated.]. 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:20304699
;
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:NP721168.RA7qBLkULtrr7ckVO8foIiaSK6mZoHpGEKip15brA_Na4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:18+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" .
}