@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP328782.RAtDtIo1vLHuVIulK-LwIBAiL0IxA2KbDXYi6jjwBxZd8
> .
@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:NP328782.RAtDtIo1vLHuVIulK-LwIBAiL0IxA2KbDXYi6jjwBxZd8130_assertion
;
np:hasProvenance
dgn-np:NP328782.RAtDtIo1vLHuVIulK-LwIBAiL0IxA2KbDXYi6jjwBxZd8130_provenance
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np:hasPublicationInfo
dgn-np:NP328782.RAtDtIo1vLHuVIulK-LwIBAiL0IxA2KbDXYi6jjwBxZd8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP328782.RAtDtIo1vLHuVIulK-LwIBAiL0IxA2KbDXYi6jjwBxZd8130_assertion
a
np:Assertion
.
dgn-np:NP328782.RAtDtIo1vLHuVIulK-LwIBAiL0IxA2KbDXYi6jjwBxZd8130_provenance
a
np:Provenance
.
dgn-np:NP328782.RAtDtIo1vLHuVIulK-LwIBAiL0IxA2KbDXYi6jjwBxZd8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP328782.RAtDtIo1vLHuVIulK-LwIBAiL0IxA2KbDXYi6jjwBxZd8130_assertion
{
miriam-gene:246744
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN9d9e83110a9d366201c5d02a2c75e802
sio:SIO_000628
miriam-gene:246744
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP328782.RAtDtIo1vLHuVIulK-LwIBAiL0IxA2KbDXYi6jjwBxZd8130_provenance
{
dgn-np:NP328782.RAtDtIo1vLHuVIulK-LwIBAiL0IxA2KbDXYi6jjwBxZd8130_assertion
dcterms:description
"[The Q7R polymorphism is unlikely to contribute significantly to Alzheimer's disease susceptibility of the Han population in south China and the variation of the Q7R polymorphism among different ethnic groups might account for the varied clinical manifestations of some STH-related diseases.]. 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:18850062
;
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:NP328782.RAtDtIo1vLHuVIulK-LwIBAiL0IxA2KbDXYi6jjwBxZd8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:13+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" .
}