@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP698784.RAR7dYZJ5L-eQQwcC5An-aTerhXULTyedsnZFFXON07BA
> .
@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:NP698784.RAR7dYZJ5L-eQQwcC5An-aTerhXULTyedsnZFFXON07BA130_head
{
this:
np:hasAssertion
dgn-np:NP698784.RAR7dYZJ5L-eQQwcC5An-aTerhXULTyedsnZFFXON07BA130_assertion
;
np:hasProvenance
dgn-np:NP698784.RAR7dYZJ5L-eQQwcC5An-aTerhXULTyedsnZFFXON07BA130_provenance
;
np:hasPublicationInfo
dgn-np:NP698784.RAR7dYZJ5L-eQQwcC5An-aTerhXULTyedsnZFFXON07BA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP698784.RAR7dYZJ5L-eQQwcC5An-aTerhXULTyedsnZFFXON07BA130_assertion
a
np:Assertion
.
dgn-np:NP698784.RAR7dYZJ5L-eQQwcC5An-aTerhXULTyedsnZFFXON07BA130_provenance
a
np:Provenance
.
dgn-np:NP698784.RAR7dYZJ5L-eQQwcC5An-aTerhXULTyedsnZFFXON07BA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP698784.RAR7dYZJ5L-eQQwcC5An-aTerhXULTyedsnZFFXON07BA130_assertion
{
miriam-gene:189
a
ncit:C16612
.
lld:C0035455
a
ncit:C7057
.
dgn-gda:DGN57d4872e467c1703d90e433a87a60c9d
sio:SIO_000628
miriam-gene:189
,
lld:C0035455
;
a
sio:SIO_001121
.
}
dgn-np:NP698784.RAR7dYZJ5L-eQQwcC5An-aTerhXULTyedsnZFFXON07BA130_provenance
{
dgn-np:NP698784.RAR7dYZJ5L-eQQwcC5An-aTerhXULTyedsnZFFXON07BA130_assertion
dcterms:description
"[The frequency of IGHG genes was similar in children with maternal and paternal heredity and in children with wheezing, eczema or rhinitis, as well as in children with different positive SPT.]. 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:17177686
;
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:NP698784.RAR7dYZJ5L-eQQwcC5An-aTerhXULTyedsnZFFXON07BA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:05+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" .
}