@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc
> .
@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:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_head
{
this:
np:hasAssertion
dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_assertion
;
np:hasProvenance
dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_provenance
;
np:hasPublicationInfo
dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_assertion
a
np:Assertion
.
dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_provenance
a
np:Provenance
.
dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_assertion
{
miriam-gene:7099
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN2ffd987e96daa6b38653989354bf6097
sio:SIO_000628
miriam-gene:7099
,
lld:C0010674
;
a
sio:SIO_001122
.
}
dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_provenance
{
dgn-np:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_assertion
dcterms:description
"[Potential reasons for absence of modifier effect include the basolateral location of TLR4 receptors on respiratory epithelium, or because inflammatory response to PA in the CF airway is so overwhelming that even a blunted response (as suggested for the 299G allele) results in increased inflammation and lung damage.]. 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:16830219
;
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:NP66759.RAesbWaQmGDOFsiLLNnAQSU18YEJhBtnxJPo4rbDvZxFc130_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
;
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" .
}