@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP670790.RA2Y5LEI2Q2RM7tAf3Pme9FaF9FL7WUxipnDkm7Zvn7co
> .
@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:NP670790.RA2Y5LEI2Q2RM7tAf3Pme9FaF9FL7WUxipnDkm7Zvn7co130_head
{
this:
np:hasAssertion
dgn-np:NP670790.RA2Y5LEI2Q2RM7tAf3Pme9FaF9FL7WUxipnDkm7Zvn7co130_assertion
;
np:hasProvenance
dgn-np:NP670790.RA2Y5LEI2Q2RM7tAf3Pme9FaF9FL7WUxipnDkm7Zvn7co130_provenance
;
np:hasPublicationInfo
dgn-np:NP670790.RA2Y5LEI2Q2RM7tAf3Pme9FaF9FL7WUxipnDkm7Zvn7co130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP670790.RA2Y5LEI2Q2RM7tAf3Pme9FaF9FL7WUxipnDkm7Zvn7co130_assertion
a
np:Assertion
.
dgn-np:NP670790.RA2Y5LEI2Q2RM7tAf3Pme9FaF9FL7WUxipnDkm7Zvn7co130_provenance
a
np:Provenance
.
dgn-np:NP670790.RA2Y5LEI2Q2RM7tAf3Pme9FaF9FL7WUxipnDkm7Zvn7co130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP670790.RA2Y5LEI2Q2RM7tAf3Pme9FaF9FL7WUxipnDkm7Zvn7co130_assertion
{
miriam-gene:4068
a
ncit:C16612
.
lld:C1304470
a
ncit:C7057
.
dgn-gda:DGNb8bbd263b153d7cd6bd90b2645d82b4e
sio:SIO_000628
miriam-gene:4068
,
lld:C1304470
;
a
sio:SIO_001121
.
}
dgn-np:NP670790.RA2Y5LEI2Q2RM7tAf3Pme9FaF9FL7WUxipnDkm7Zvn7co130_provenance
{
dgn-np:NP670790.RA2Y5LEI2Q2RM7tAf3Pme9FaF9FL7WUxipnDkm7Zvn7co130_assertion
dcterms:description
"[The results indicate that the LYP missense R620W polymorphism may have an influence on the development of generalised vitiligo and provide further evidence for autoimmunity as an aetiological factor with respect to this disease.]. 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:16015369
;
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:NP670790.RA2Y5LEI2Q2RM7tAf3Pme9FaF9FL7WUxipnDkm7Zvn7co130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:45+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" .
}