@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP904519.RAgxg88gbFlu80LxYKsIefm1xdWK4MPE4LLxd3cqnCnHA
> .
@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:NP904519.RAgxg88gbFlu80LxYKsIefm1xdWK4MPE4LLxd3cqnCnHA130_head
{
this:
np:hasAssertion
dgn-np:NP904519.RAgxg88gbFlu80LxYKsIefm1xdWK4MPE4LLxd3cqnCnHA130_assertion
;
np:hasProvenance
dgn-np:NP904519.RAgxg88gbFlu80LxYKsIefm1xdWK4MPE4LLxd3cqnCnHA130_provenance
;
np:hasPublicationInfo
dgn-np:NP904519.RAgxg88gbFlu80LxYKsIefm1xdWK4MPE4LLxd3cqnCnHA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP904519.RAgxg88gbFlu80LxYKsIefm1xdWK4MPE4LLxd3cqnCnHA130_assertion
a
np:Assertion
.
dgn-np:NP904519.RAgxg88gbFlu80LxYKsIefm1xdWK4MPE4LLxd3cqnCnHA130_provenance
a
np:Provenance
.
dgn-np:NP904519.RAgxg88gbFlu80LxYKsIefm1xdWK4MPE4LLxd3cqnCnHA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP904519.RAgxg88gbFlu80LxYKsIefm1xdWK4MPE4LLxd3cqnCnHA130_assertion
{
miriam-gene:6352
a
ncit:C16612
.
lld:C0001883
a
ncit:C7057
.
dgn-gda:DGNc88c7949740806e0b1e87f3ee604fc3b
sio:SIO_000628
miriam-gene:6352
,
lld:C0001883
;
a
sio:SIO_001121
.
}
dgn-np:NP904519.RAgxg88gbFlu80LxYKsIefm1xdWK4MPE4LLxd3cqnCnHA130_provenance
{
dgn-np:NP904519.RAgxg88gbFlu80LxYKsIefm1xdWK4MPE4LLxd3cqnCnHA130_assertion
dcterms:description
"[Many studies have made an interesting link between RANTES polymorphisms and asthma, showing that the variant in the promoter region is associated with high risk of asthma and severe airway obstruction.]. 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:17678722
;
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:NP904519.RAgxg88gbFlu80LxYKsIefm1xdWK4MPE4LLxd3cqnCnHA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:15+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" .
}