@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP385521.RA1sKBOblTXJO33GRpdjqMt4ooQ8pO8q8u3It0J03Q5EQ
> .
@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:NP385521.RA1sKBOblTXJO33GRpdjqMt4ooQ8pO8q8u3It0J03Q5EQ130_head
{
this:
np:hasAssertion
dgn-np:NP385521.RA1sKBOblTXJO33GRpdjqMt4ooQ8pO8q8u3It0J03Q5EQ130_assertion
;
np:hasProvenance
dgn-np:NP385521.RA1sKBOblTXJO33GRpdjqMt4ooQ8pO8q8u3It0J03Q5EQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP385521.RA1sKBOblTXJO33GRpdjqMt4ooQ8pO8q8u3It0J03Q5EQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP385521.RA1sKBOblTXJO33GRpdjqMt4ooQ8pO8q8u3It0J03Q5EQ130_assertion
a
np:Assertion
.
dgn-np:NP385521.RA1sKBOblTXJO33GRpdjqMt4ooQ8pO8q8u3It0J03Q5EQ130_provenance
a
np:Provenance
.
dgn-np:NP385521.RA1sKBOblTXJO33GRpdjqMt4ooQ8pO8q8u3It0J03Q5EQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP385521.RA1sKBOblTXJO33GRpdjqMt4ooQ8pO8q8u3It0J03Q5EQ130_assertion
{
miriam-gene:8000
a
ncit:C16612
.
lld:C0699885
a
ncit:C7057
.
dgn-gda:DGNdf2f8fccc2d25b2ccf95ecb4e4240fbf
sio:SIO_000628
miriam-gene:8000
,
lld:C0699885
;
a
sio:SIO_001121
.
}
dgn-np:NP385521.RA1sKBOblTXJO33GRpdjqMt4ooQ8pO8q8u3It0J03Q5EQ130_provenance
{
dgn-np:NP385521.RA1sKBOblTXJO33GRpdjqMt4ooQ8pO8q8u3It0J03Q5EQ130_assertion
dcterms:description
"[In conclusion, a joint effect of two PSCA SNPs, rs2294008 and rs2978974, suggests that both variants may be important for bladder cancer susceptibility, possibly through different mechanisms that influence the control of mRNA expression and interaction with regulatory factors.]. 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:22416122
;
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:NP385521.RA1sKBOblTXJO33GRpdjqMt4ooQ8pO8q8u3It0J03Q5EQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:49+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" .
}