@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP677793.RAVtR3p1ntLj5u_87afdVTcZXL2C7TbKyrjSE7237qnCA
> .
@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:NP677793.RAVtR3p1ntLj5u_87afdVTcZXL2C7TbKyrjSE7237qnCA130_head
{
this:
np:hasAssertion
dgn-np:NP677793.RAVtR3p1ntLj5u_87afdVTcZXL2C7TbKyrjSE7237qnCA130_assertion
;
np:hasProvenance
dgn-np:NP677793.RAVtR3p1ntLj5u_87afdVTcZXL2C7TbKyrjSE7237qnCA130_provenance
;
np:hasPublicationInfo
dgn-np:NP677793.RAVtR3p1ntLj5u_87afdVTcZXL2C7TbKyrjSE7237qnCA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP677793.RAVtR3p1ntLj5u_87afdVTcZXL2C7TbKyrjSE7237qnCA130_assertion
a
np:Assertion
.
dgn-np:NP677793.RAVtR3p1ntLj5u_87afdVTcZXL2C7TbKyrjSE7237qnCA130_provenance
a
np:Provenance
.
dgn-np:NP677793.RAVtR3p1ntLj5u_87afdVTcZXL2C7TbKyrjSE7237qnCA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP677793.RAVtR3p1ntLj5u_87afdVTcZXL2C7TbKyrjSE7237qnCA130_assertion
{
miriam-gene:3579
a
ncit:C16612
.
lld:C0024115
a
ncit:C7057
.
dgn-gda:DGNaa6a87b8df2fe1aa0185f16675294d60
sio:SIO_000628
miriam-gene:3579
,
lld:C0024115
;
a
sio:SIO_001121
.
}
dgn-np:NP677793.RAVtR3p1ntLj5u_87afdVTcZXL2C7TbKyrjSE7237qnCA130_provenance
{
dgn-np:NP677793.RAVtR3p1ntLj5u_87afdVTcZXL2C7TbKyrjSE7237qnCA130_assertion
dcterms:description
"[With the development of several pharmacological, immunological and genetic tools to study CXCR2 function, an important role for this CXC chemokine receptor subtype has been identified in chronic obstructive pulmonary disease (COPD), asthma and fibrotic pulmonary disorders.]. 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:19026683
;
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:NP677793.RAVtR3p1ntLj5u_87afdVTcZXL2C7TbKyrjSE7237qnCA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:49+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" .
}