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http://rdf.disgenet.org/nanopublications.trig#NP662101.RAA9HtoD73OMvEe6NKucwpZ_iMzcMw9bYcVYa5l__DN1g
> .
@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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP662101.RAA9HtoD73OMvEe6NKucwpZ_iMzcMw9bYcVYa5l__DN1g130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
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;
a
np:Nanopublication
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dgn-np:NP662101.RAA9HtoD73OMvEe6NKucwpZ_iMzcMw9bYcVYa5l__DN1g130_assertion
a
np:Assertion
.
dgn-np:NP662101.RAA9HtoD73OMvEe6NKucwpZ_iMzcMw9bYcVYa5l__DN1g130_provenance
a
np:Provenance
.
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a
np:PublicationInfo
.
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dgn-np:NP662101.RAA9HtoD73OMvEe6NKucwpZ_iMzcMw9bYcVYa5l__DN1g130_assertion
{
miriam-gene:4261
a
ncit:C16612
.
lld:C0011615
a
ncit:C7057
.
dgn-gda:DGNa06ac231873f322fc4b42c939e523b8f
sio:SIO_000628
miriam-gene:4261
,
lld:C0011615
;
a
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.
}
dgn-np:NP662101.RAA9HtoD73OMvEe6NKucwpZ_iMzcMw9bYcVYa5l__DN1g130_provenance
{
dgn-np:NP662101.RAA9HtoD73OMvEe6NKucwpZ_iMzcMw9bYcVYa5l__DN1g130_assertion
dcterms:description
"[In order to investigate the role of variation in NLR genes for AD, we genotyped 23 single nucleotide polymorphisms (SNPs) in seven selected NLR genes (CARD4, CARD15, CARD12, NALP1, NALP3, NALP12, MHC2TA) in 392 AD patients and 297 controls by restriction enzyme digestion or TaqMan assays.]. 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:17620097
;
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:NP662101.RAA9HtoD73OMvEe6NKucwpZ_iMzcMw9bYcVYa5l__DN1g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:40+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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> , <
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" .
}