@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP65774.RABNhx5r7euBtre_x_7t6XGM_R0Ai2cVVkRX_0ARPeqYY
> .
@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:NP65774.RABNhx5r7euBtre_x_7t6XGM_R0Ai2cVVkRX_0ARPeqYY130_head
{
this:
np:hasAssertion
dgn-np:NP65774.RABNhx5r7euBtre_x_7t6XGM_R0Ai2cVVkRX_0ARPeqYY130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP65774.RABNhx5r7euBtre_x_7t6XGM_R0Ai2cVVkRX_0ARPeqYY130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP65774.RABNhx5r7euBtre_x_7t6XGM_R0Ai2cVVkRX_0ARPeqYY130_assertion
a
np:Assertion
.
dgn-np:NP65774.RABNhx5r7euBtre_x_7t6XGM_R0Ai2cVVkRX_0ARPeqYY130_provenance
a
np:Provenance
.
dgn-np:NP65774.RABNhx5r7euBtre_x_7t6XGM_R0Ai2cVVkRX_0ARPeqYY130_publicationInfo
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dgn-np:NP65774.RABNhx5r7euBtre_x_7t6XGM_R0Ai2cVVkRX_0ARPeqYY130_assertion
{
miriam-gene:4318
a
ncit:C16612
.
lld:C0005684
a
ncit:C7057
.
dgn-gda:DGNd7dba034df65f7eae7cffab8f305fdf4
sio:SIO_000628
miriam-gene:4318
,
lld:C0005684
;
a
sio:SIO_001122
.
}
dgn-np:NP65774.RABNhx5r7euBtre_x_7t6XGM_R0Ai2cVVkRX_0ARPeqYY130_provenance
{
dgn-np:NP65774.RABNhx5r7euBtre_x_7t6XGM_R0Ai2cVVkRX_0ARPeqYY130_assertion
dcterms:description
"[Using a case-only study, we examined the association of 11 single-nucleotide polymorphisms and one microsatellite polymorphism in MMP genes MMP1, MMP2, MMP3, MMP8, MMP9, and MMP12 with the risk of invasive bladder cancer in 243 Caucasian patients with muscle invasive compared with 315 Caucasian patients with superficial disease.]. 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:17473191
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP65774.RABNhx5r7euBtre_x_7t6XGM_R0Ai2cVVkRX_0ARPeqYY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:31+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
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pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
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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
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"v2.1.0" .
}