@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP429765.RA3JZhSDMr4XaFvNfZm0zuEPKDzCIfdiLFlxTAKCCccXA
> .
@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:NP429765.RA3JZhSDMr4XaFvNfZm0zuEPKDzCIfdiLFlxTAKCCccXA130_head
{
this:
np:hasAssertion
dgn-np:NP429765.RA3JZhSDMr4XaFvNfZm0zuEPKDzCIfdiLFlxTAKCCccXA130_assertion
;
np:hasProvenance
dgn-np:NP429765.RA3JZhSDMr4XaFvNfZm0zuEPKDzCIfdiLFlxTAKCCccXA130_provenance
;
np:hasPublicationInfo
dgn-np:NP429765.RA3JZhSDMr4XaFvNfZm0zuEPKDzCIfdiLFlxTAKCCccXA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP429765.RA3JZhSDMr4XaFvNfZm0zuEPKDzCIfdiLFlxTAKCCccXA130_assertion
a
np:Assertion
.
dgn-np:NP429765.RA3JZhSDMr4XaFvNfZm0zuEPKDzCIfdiLFlxTAKCCccXA130_provenance
a
np:Provenance
.
dgn-np:NP429765.RA3JZhSDMr4XaFvNfZm0zuEPKDzCIfdiLFlxTAKCCccXA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP429765.RA3JZhSDMr4XaFvNfZm0zuEPKDzCIfdiLFlxTAKCCccXA130_assertion
{
miriam-gene:57016
a
ncit:C16612
.
lld:C0028043
a
ncit:C7057
.
dgn-gda:DGN86dcf8dcdef3123779b32b6b8232b224
sio:SIO_000628
miriam-gene:57016
,
lld:C0028043
;
a
sio:SIO_001121
.
}
dgn-np:NP429765.RA3JZhSDMr4XaFvNfZm0zuEPKDzCIfdiLFlxTAKCCccXA130_provenance
{
dgn-np:NP429765.RA3JZhSDMr4XaFvNfZm0zuEPKDzCIfdiLFlxTAKCCccXA130_assertion
dcterms:description
"[In this study, we analyzed 21 single nucleotide polymorphisms (SNPs) within NRXN1 for association with ND, which was assessed by smoking quantity (SQ), the heaviness of smoking index (HSI) and the Fagerström test for ND (FTND).]. 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:18270208
;
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:NP429765.RA3JZhSDMr4XaFvNfZm0zuEPKDzCIfdiLFlxTAKCCccXA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:14+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" .
}