@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP511208.RAT6LdHl8Uo0nwK8BEtvXiasIGE44MmFh9GFl8yPIcYcA
> .
@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:NP511208.RAT6LdHl8Uo0nwK8BEtvXiasIGE44MmFh9GFl8yPIcYcA130_head
{
this:
np:hasAssertion
dgn-np:NP511208.RAT6LdHl8Uo0nwK8BEtvXiasIGE44MmFh9GFl8yPIcYcA130_assertion
;
np:hasProvenance
dgn-np:NP511208.RAT6LdHl8Uo0nwK8BEtvXiasIGE44MmFh9GFl8yPIcYcA130_provenance
;
np:hasPublicationInfo
dgn-np:NP511208.RAT6LdHl8Uo0nwK8BEtvXiasIGE44MmFh9GFl8yPIcYcA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP511208.RAT6LdHl8Uo0nwK8BEtvXiasIGE44MmFh9GFl8yPIcYcA130_assertion
a
np:Assertion
.
dgn-np:NP511208.RAT6LdHl8Uo0nwK8BEtvXiasIGE44MmFh9GFl8yPIcYcA130_provenance
a
np:Provenance
.
dgn-np:NP511208.RAT6LdHl8Uo0nwK8BEtvXiasIGE44MmFh9GFl8yPIcYcA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP511208.RAT6LdHl8Uo0nwK8BEtvXiasIGE44MmFh9GFl8yPIcYcA130_assertion
{
miriam-gene:930
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGNc9f853bcb539dd65124a20a3eda89633
sio:SIO_000628
miriam-gene:930
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP511208.RAT6LdHl8Uo0nwK8BEtvXiasIGE44MmFh9GFl8yPIcYcA130_provenance
{
dgn-np:NP511208.RAT6LdHl8Uo0nwK8BEtvXiasIGE44MmFh9GFl8yPIcYcA130_assertion
dcterms:description
"[Several new associations have been disclosed, including those of TNFR2, FCGR2B, and CD19 gene polymorphisms with systemic lupus erythematosus, in addition to some unexpected findings such as the common occurrence of NKG2-C null allele in the healthy population.]. 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:12493014
;
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:NP511208.RAT6LdHl8Uo0nwK8BEtvXiasIGE44MmFh9GFl8yPIcYcA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:04+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" .
}