@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM
> .
@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:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_head
{
this:
np:hasAssertion
dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_assertion
;
np:hasProvenance
dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_provenance
;
np:hasPublicationInfo
dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_assertion
a
np:Assertion
.
dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_provenance
a
np:Provenance
.
dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_assertion
{
miriam-gene:3577
a
ncit:C16612
.
lld:C0034186
a
ncit:C7057
.
dgn-gda:DGNb0ec6292e67851f5988ea57b31f9d1fc
sio:SIO_000628
miriam-gene:3577
,
lld:C0034186
;
a
sio:SIO_001121
.
}
dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_provenance
{
dgn-np:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_assertion
dcterms:description
"[Here we discuss the mechanisms of neutrophil-mediated, chemokine receptor (CXCR1)-dependent clearance, and the defect in interleukin-8 receptor homolog knock-out (IL-8Rh KO) mice and describe the data linking low CXCR1 expression to recurrent pyelonephritis in man, as well as the information on the genetic basis for low CXCR1 expression in affected patients.]. 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:11817650
;
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:NP824397.RA1LHj6A2fUrfdmmL59eaSk5fpdEmPUegzvVgioXm52FM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:25+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" .
}