@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP227817.RAualYYTgAFpjfR1hUNtgWj752RdDmGTqPtzwsX8zRikg
> .
@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:NP227817.RAualYYTgAFpjfR1hUNtgWj752RdDmGTqPtzwsX8zRikg130_head
{
this:
np:hasAssertion
dgn-np:NP227817.RAualYYTgAFpjfR1hUNtgWj752RdDmGTqPtzwsX8zRikg130_assertion
;
np:hasProvenance
dgn-np:NP227817.RAualYYTgAFpjfR1hUNtgWj752RdDmGTqPtzwsX8zRikg130_provenance
;
np:hasPublicationInfo
dgn-np:NP227817.RAualYYTgAFpjfR1hUNtgWj752RdDmGTqPtzwsX8zRikg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP227817.RAualYYTgAFpjfR1hUNtgWj752RdDmGTqPtzwsX8zRikg130_assertion
a
np:Assertion
.
dgn-np:NP227817.RAualYYTgAFpjfR1hUNtgWj752RdDmGTqPtzwsX8zRikg130_provenance
a
np:Provenance
.
dgn-np:NP227817.RAualYYTgAFpjfR1hUNtgWj752RdDmGTqPtzwsX8zRikg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP227817.RAualYYTgAFpjfR1hUNtgWj752RdDmGTqPtzwsX8zRikg130_assertion
{
miriam-gene:2215
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGN51f362a8916f8766f365bc84dda81fb3
sio:SIO_000628
miriam-gene:2215
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP227817.RAualYYTgAFpjfR1hUNtgWj752RdDmGTqPtzwsX8zRikg130_provenance
{
dgn-np:NP227817.RAualYYTgAFpjfR1hUNtgWj752RdDmGTqPtzwsX8zRikg130_assertion
dcterms:description
"[The human neutrophil antigen-1 allotypes of FcgammaRIIIB and the role of the receptor in SLE are discussed with regard to the recent determination of copy number variation in FCGR3B and the association of low copy number with SLE.]. 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:20146709
;
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:NP227817.RAualYYTgAFpjfR1hUNtgWj752RdDmGTqPtzwsX8zRikg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:06+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" .
}