@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ
> .
@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:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_head
{
this:
np:hasAssertion
dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_assertion
;
np:hasProvenance
dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_assertion
a
np:Assertion
.
dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_provenance
a
np:Provenance
.
dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_assertion
{
miriam-gene:3565
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGNeaa29bbc74382d5ded593624eb30a608
sio:SIO_000628
miriam-gene:3565
,
lld:C0004096
;
a
sio:SIO_001121
.
}
dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_provenance
{
dgn-np:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_assertion
dcterms:description
"[Because populations of African descent have increased levels of genetic variation compared with other populations, particularly with respect to low frequency or rare variants, we hypothesized that rare variants in the IL4 gene contribute to the development of asthma in African Americans.]. 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:19910025
;
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:NP200451.RA4krlU6fSM8-B2I5eEVLsbuZ6mHXntPlnNEXQ7znDbBQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:50+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" .
}