@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc
> .
@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:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_head
{
this:
np:hasAssertion
dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_assertion
;
np:hasProvenance
dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_provenance
;
np:hasPublicationInfo
dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_assertion
a
np:Assertion
.
dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_provenance
a
np:Provenance
.
dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_assertion
{
miriam-gene:3991
a
ncit:C16612
.
lld:C0024117
a
ncit:C7057
.
dgn-gda:DGNd743317eb4769173c6fdb177b5f37313
sio:SIO_000628
miriam-gene:3991
,
lld:C0024117
;
a
sio:SIO_001121
.
}
dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_provenance
{
dgn-np:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_assertion
dcterms:description
"[Polymorphisms that were associated with lung function level or rate of decline in the Lung Health Study (LHS) cohort were analyzed for association with COPD affection status in four other COPD case-control populations.]. 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:22200767
;
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:NP398476.RAI_42R449ZvRmqBnFZsVVjef92CCmQ0dZ20xv3trAwsc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:57+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" .
}