@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP395890.RA3U-Itl_nkcep08RY9iDTW6PxydaeX2AB1DMMt1ztCA4
> .
@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:NP395890.RA3U-Itl_nkcep08RY9iDTW6PxydaeX2AB1DMMt1ztCA4130_head
{
this:
np:hasAssertion
dgn-np:NP395890.RA3U-Itl_nkcep08RY9iDTW6PxydaeX2AB1DMMt1ztCA4130_assertion
;
np:hasProvenance
dgn-np:NP395890.RA3U-Itl_nkcep08RY9iDTW6PxydaeX2AB1DMMt1ztCA4130_provenance
;
np:hasPublicationInfo
dgn-np:NP395890.RA3U-Itl_nkcep08RY9iDTW6PxydaeX2AB1DMMt1ztCA4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP395890.RA3U-Itl_nkcep08RY9iDTW6PxydaeX2AB1DMMt1ztCA4130_assertion
a
np:Assertion
.
dgn-np:NP395890.RA3U-Itl_nkcep08RY9iDTW6PxydaeX2AB1DMMt1ztCA4130_provenance
a
np:Provenance
.
dgn-np:NP395890.RA3U-Itl_nkcep08RY9iDTW6PxydaeX2AB1DMMt1ztCA4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP395890.RA3U-Itl_nkcep08RY9iDTW6PxydaeX2AB1DMMt1ztCA4130_assertion
{
miriam-gene:388697
a
ncit:C16612
.
lld:C0011615
a
ncit:C7057
.
dgn-gda:DGN6ac31129d499875caddce78991277ac6
sio:SIO_000628
miriam-gene:388697
,
lld:C0011615
;
a
sio:SIO_001121
.
}
dgn-np:NP395890.RA3U-Itl_nkcep08RY9iDTW6PxydaeX2AB1DMMt1ztCA4130_provenance
{
dgn-np:NP395890.RA3U-Itl_nkcep08RY9iDTW6PxydaeX2AB1DMMt1ztCA4130_assertion
dcterms:description
"[Recently, the two single nucleotide polymorphisms, rs7927894 on chromosome 11q13.5 and rs877776 within the region of the hornerin gene, were identified as novel susceptibility variants for atopic dermatitis in the first genome wide association study in atopic dermatitis.]. 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:23557745
;
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:NP395890.RA3U-Itl_nkcep08RY9iDTW6PxydaeX2AB1DMMt1ztCA4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:55+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" .
}