@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4
> .
@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:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_head
{
this:
np:hasAssertion
dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_assertion
;
np:hasProvenance
dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_provenance
;
np:hasPublicationInfo
dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_assertion
a
np:Assertion
.
dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_provenance
a
np:Provenance
.
dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_assertion
{
miriam-gene:3658
a
ncit:C16612
.
lld:C0024117
a
ncit:C7057
.
dgn-gda:DGNb385944eefe626f4c015062e8ea6eb48
sio:SIO_000628
miriam-gene:3658
,
lld:C0024117
;
a
sio:SIO_001121
.
}
dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_provenance
{
dgn-np:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_assertion
dcterms:description
"[Genome-wide association studies and integrative genomics approaches in COPD have demonstrated significant associations with SNPs in the chromosome 15q region that includes CHRNA3 (cholinergic nicotine receptor alpha3) and IREB2 (iron regulatory binding protein 2).We investigated whether SNPs in the chromosome 15q region would be modifiers for lung function and COPD in AAT deficiency.]. 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:22356581
;
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:NP675355.RA_28B03gTO1yTC2_Afg8xNgUJDBbDJmn538mlhXAu1T4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:47+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" .
}