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http://rdf.disgenet.org/nanopublications.trig#NP50331.RAIsXCm54FuusNE02nv3_PoNXDrqFSrJkJzOlJKRWGbP8
> .
@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
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np:hasProvenance
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dgn-np:NP50331.RAIsXCm54FuusNE02nv3_PoNXDrqFSrJkJzOlJKRWGbP8130_publicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP50331.RAIsXCm54FuusNE02nv3_PoNXDrqFSrJkJzOlJKRWGbP8130_provenance
a
np:Provenance
.
dgn-np:NP50331.RAIsXCm54FuusNE02nv3_PoNXDrqFSrJkJzOlJKRWGbP8130_publicationInfo
a
np:PublicationInfo
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{
miriam-gene:7124
a
ncit:C16612
.
lld:C0013990
a
ncit:C7057
.
dgn-gda:DGNc662683b38bf52958f91f15c7d8969c3
sio:SIO_000628
miriam-gene:7124
,
lld:C0013990
;
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.
}
dgn-np:NP50331.RAIsXCm54FuusNE02nv3_PoNXDrqFSrJkJzOlJKRWGbP8130_provenance
{
dgn-np:NP50331.RAIsXCm54FuusNE02nv3_PoNXDrqFSrJkJzOlJKRWGbP8130_assertion
dcterms:description
"[No significant deviations were found concerning the four polymorphisms studied between the two populations. The authors confirm that the tumour necrosis factor family genes, at least for the polymorphisms investigated, are not major genetic risk factors for chronic obstructive pulmonary disease in Caucasians, either defined in terms of emphysema (this study) or airflow obstruction (previous studies). Nevertheless, the authors would like to emphasise the importance of narrowing the phenotype in the search for genetic risk factors in chronic obstructive pulmonary disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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sio:SIO_000772
miriam-pubmed:12661999
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;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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 .
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dgn-np:NP50331.RAIsXCm54FuusNE02nv3_PoNXDrqFSrJkJzOlJKRWGbP8130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
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> , <
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> , <
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<
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