@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP400477.RAHdVsutTF-SyyqunpIEMDem0hb5R8Lp1XWCVCeIV4f54
> .
@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:NP400477.RAHdVsutTF-SyyqunpIEMDem0hb5R8Lp1XWCVCeIV4f54130_head
{
this:
np:hasAssertion
dgn-np:NP400477.RAHdVsutTF-SyyqunpIEMDem0hb5R8Lp1XWCVCeIV4f54130_assertion
;
np:hasProvenance
dgn-np:NP400477.RAHdVsutTF-SyyqunpIEMDem0hb5R8Lp1XWCVCeIV4f54130_provenance
;
np:hasPublicationInfo
dgn-np:NP400477.RAHdVsutTF-SyyqunpIEMDem0hb5R8Lp1XWCVCeIV4f54130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP400477.RAHdVsutTF-SyyqunpIEMDem0hb5R8Lp1XWCVCeIV4f54130_assertion
a
np:Assertion
.
dgn-np:NP400477.RAHdVsutTF-SyyqunpIEMDem0hb5R8Lp1XWCVCeIV4f54130_provenance
a
np:Provenance
.
dgn-np:NP400477.RAHdVsutTF-SyyqunpIEMDem0hb5R8Lp1XWCVCeIV4f54130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP400477.RAHdVsutTF-SyyqunpIEMDem0hb5R8Lp1XWCVCeIV4f54130_assertion
{
miriam-gene:3596
a
ncit:C16612
.
lld:C0043144
a
ncit:C7057
.
dgn-gda:DGNec0e4b44d6fdeba536618b0ad99072d6
sio:SIO_000628
miriam-gene:3596
,
lld:C0043144
;
a
sio:SIO_001121
.
}
dgn-np:NP400477.RAHdVsutTF-SyyqunpIEMDem0hb5R8Lp1XWCVCeIV4f54130_provenance
{
dgn-np:NP400477.RAHdVsutTF-SyyqunpIEMDem0hb5R8Lp1XWCVCeIV4f54130_assertion
dcterms:description
"[We were unable to confirm associations of the positional candidates DPP10 and PHF11 with wheeze, although our study had ample power to detect the expected associations of IL13 variants with IgE and SPINK5 variants with eczema.]. 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:20085599
;
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:NP400477.RAHdVsutTF-SyyqunpIEMDem0hb5R8Lp1XWCVCeIV4f54130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:58+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" .
}