@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP814616.RAwVtH_nLOdpKudYIPEbUM63zbP2eYbCbew1NJXw-nd9k
> .
@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:NP814616.RAwVtH_nLOdpKudYIPEbUM63zbP2eYbCbew1NJXw-nd9k130_head
{
this:
np:hasAssertion
dgn-np:NP814616.RAwVtH_nLOdpKudYIPEbUM63zbP2eYbCbew1NJXw-nd9k130_assertion
;
np:hasProvenance
dgn-np:NP814616.RAwVtH_nLOdpKudYIPEbUM63zbP2eYbCbew1NJXw-nd9k130_provenance
;
np:hasPublicationInfo
dgn-np:NP814616.RAwVtH_nLOdpKudYIPEbUM63zbP2eYbCbew1NJXw-nd9k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP814616.RAwVtH_nLOdpKudYIPEbUM63zbP2eYbCbew1NJXw-nd9k130_assertion
a
np:Assertion
.
dgn-np:NP814616.RAwVtH_nLOdpKudYIPEbUM63zbP2eYbCbew1NJXw-nd9k130_provenance
a
np:Provenance
.
dgn-np:NP814616.RAwVtH_nLOdpKudYIPEbUM63zbP2eYbCbew1NJXw-nd9k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP814616.RAwVtH_nLOdpKudYIPEbUM63zbP2eYbCbew1NJXw-nd9k130_assertion
{
miriam-gene:2209
a
ncit:C16612
.
lld:C0003873
a
ncit:C7057
.
dgn-gda:DGNff6997a30c7ce636d7c3ade874849825
sio:SIO_000628
miriam-gene:2209
,
lld:C0003873
;
a
sio:SIO_001121
.
}
dgn-np:NP814616.RAwVtH_nLOdpKudYIPEbUM63zbP2eYbCbew1NJXw-nd9k130_provenance
{
dgn-np:NP814616.RAwVtH_nLOdpKudYIPEbUM63zbP2eYbCbew1NJXw-nd9k130_assertion
dcterms:description
"[Unlike other genetic polymorphisms reported in periodontology, most Fcγ receptor polymorphisms reported not only have established biological functions but are reported to associate with other autoimmune diseases, such as rheumatoid arthritis and systemic lupus erythematosus.]. 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:22117888
;
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:NP814616.RAwVtH_nLOdpKudYIPEbUM63zbP2eYbCbew1NJXw-nd9k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:19+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" .
}