@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP247344.RA2iF1CekfHZV1RusUjqDkeJ-EgpAH9N40Gd03sUfDB08
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP247344.RA2iF1CekfHZV1RusUjqDkeJ-EgpAH9N40Gd03sUfDB08130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP247344.RA2iF1CekfHZV1RusUjqDkeJ-EgpAH9N40Gd03sUfDB08130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP247344.RA2iF1CekfHZV1RusUjqDkeJ-EgpAH9N40Gd03sUfDB08130_assertion
a
np:Assertion
.
dgn-np:NP247344.RA2iF1CekfHZV1RusUjqDkeJ-EgpAH9N40Gd03sUfDB08130_provenance
a
np:Provenance
.
dgn-np:NP247344.RA2iF1CekfHZV1RusUjqDkeJ-EgpAH9N40Gd03sUfDB08130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:325
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN803ac5f7f811936a147fad5428c40d74
sio:SIO_000628
miriam-gene:325
,
lld:C0006826
;
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.
}
dgn-np:NP247344.RA2iF1CekfHZV1RusUjqDkeJ-EgpAH9N40Gd03sUfDB08130_provenance
{
dgn-np:NP247344.RA2iF1CekfHZV1RusUjqDkeJ-EgpAH9N40Gd03sUfDB08130_assertion
dcterms:description
"[By using SAP as the focal point of our studies, we hope to identify novel signaling pathways that could be targeted to improve the treatment for patients with XLP as well as more common disorders, such as autoimmunity and cancer.]. 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:18815745
;
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 .
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dgn-np:NP247344.RA2iF1CekfHZV1RusUjqDkeJ-EgpAH9N40Gd03sUfDB08130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:18+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
<
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> , <
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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