@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP393438.RAJHzxaK9Qy1fdp9RDIDHRoR4t53k0HyegdY5Wr09CFhE
> .
@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:NP393438.RAJHzxaK9Qy1fdp9RDIDHRoR4t53k0HyegdY5Wr09CFhE130_head
{
this:
np:hasAssertion
dgn-np:NP393438.RAJHzxaK9Qy1fdp9RDIDHRoR4t53k0HyegdY5Wr09CFhE130_assertion
;
np:hasProvenance
dgn-np:NP393438.RAJHzxaK9Qy1fdp9RDIDHRoR4t53k0HyegdY5Wr09CFhE130_provenance
;
np:hasPublicationInfo
dgn-np:NP393438.RAJHzxaK9Qy1fdp9RDIDHRoR4t53k0HyegdY5Wr09CFhE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP393438.RAJHzxaK9Qy1fdp9RDIDHRoR4t53k0HyegdY5Wr09CFhE130_assertion
a
np:Assertion
.
dgn-np:NP393438.RAJHzxaK9Qy1fdp9RDIDHRoR4t53k0HyegdY5Wr09CFhE130_provenance
a
np:Provenance
.
dgn-np:NP393438.RAJHzxaK9Qy1fdp9RDIDHRoR4t53k0HyegdY5Wr09CFhE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP393438.RAJHzxaK9Qy1fdp9RDIDHRoR4t53k0HyegdY5Wr09CFhE130_assertion
{
miriam-gene:26191
a
ncit:C16612
.
lld:C0041327
a
ncit:C7057
.
dgn-gda:DGN5c94eda4081ae44d7f61d2388bc9b570
sio:SIO_000628
miriam-gene:26191
,
lld:C0041327
;
a
sio:SIO_001121
.
}
dgn-np:NP393438.RAJHzxaK9Qy1fdp9RDIDHRoR4t53k0HyegdY5Wr09CFhE130_provenance
{
dgn-np:NP393438.RAJHzxaK9Qy1fdp9RDIDHRoR4t53k0HyegdY5Wr09CFhE130_assertion
dcterms:description
"[The purpose of this study was to investigate the role of two functional missense single nucleotide polymorphisms (SNPs) of the PTPN22 gene region (R620W and R263Q) in the susceptibility to TB in the Moroccan population.]. 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:19563523
;
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:NP393438.RAJHzxaK9Qy1fdp9RDIDHRoR4t53k0HyegdY5Wr09CFhE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:54+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" .
}