@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP258902.RAWiHtKapqs1FsNSqOaXoViBY73zDN6WgeN8S9SIVGYk0
> .
@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:NP258902.RAWiHtKapqs1FsNSqOaXoViBY73zDN6WgeN8S9SIVGYk0130_head
{
this:
np:hasAssertion
dgn-np:NP258902.RAWiHtKapqs1FsNSqOaXoViBY73zDN6WgeN8S9SIVGYk0130_assertion
;
np:hasProvenance
dgn-np:NP258902.RAWiHtKapqs1FsNSqOaXoViBY73zDN6WgeN8S9SIVGYk0130_provenance
;
np:hasPublicationInfo
dgn-np:NP258902.RAWiHtKapqs1FsNSqOaXoViBY73zDN6WgeN8S9SIVGYk0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP258902.RAWiHtKapqs1FsNSqOaXoViBY73zDN6WgeN8S9SIVGYk0130_assertion
a
np:Assertion
.
dgn-np:NP258902.RAWiHtKapqs1FsNSqOaXoViBY73zDN6WgeN8S9SIVGYk0130_provenance
a
np:Provenance
.
dgn-np:NP258902.RAWiHtKapqs1FsNSqOaXoViBY73zDN6WgeN8S9SIVGYk0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP258902.RAWiHtKapqs1FsNSqOaXoViBY73zDN6WgeN8S9SIVGYk0130_assertion
{
miriam-gene:3594
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN1305ecb8fb158b37212dafda86fcc230
sio:SIO_000628
miriam-gene:3594
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP258902.RAWiHtKapqs1FsNSqOaXoViBY73zDN6WgeN8S9SIVGYk0130_provenance
{
dgn-np:NP258902.RAWiHtKapqs1FsNSqOaXoViBY73zDN6WgeN8S9SIVGYk0130_assertion
dcterms:description
"[Rare variants in IL12RB1 were also associated with asthma susceptibility among European Americans, despite the fact that the majority of rare variants in IL12RB1 were specific to either one of the 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:22325360
;
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:NP258902.RAWiHtKapqs1FsNSqOaXoViBY73zDN6WgeN8S9SIVGYk0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:24+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" .
}