@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP392756.RAPLOt6ykB-OfZMf0jtYSmTfQJrrYsXy12j76gtdAOn7I
> .
@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:NP392756.RAPLOt6ykB-OfZMf0jtYSmTfQJrrYsXy12j76gtdAOn7I130_head
{
this:
np:hasAssertion
dgn-np:NP392756.RAPLOt6ykB-OfZMf0jtYSmTfQJrrYsXy12j76gtdAOn7I130_assertion
;
np:hasProvenance
dgn-np:NP392756.RAPLOt6ykB-OfZMf0jtYSmTfQJrrYsXy12j76gtdAOn7I130_provenance
;
np:hasPublicationInfo
dgn-np:NP392756.RAPLOt6ykB-OfZMf0jtYSmTfQJrrYsXy12j76gtdAOn7I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP392756.RAPLOt6ykB-OfZMf0jtYSmTfQJrrYsXy12j76gtdAOn7I130_assertion
a
np:Assertion
.
dgn-np:NP392756.RAPLOt6ykB-OfZMf0jtYSmTfQJrrYsXy12j76gtdAOn7I130_provenance
a
np:Provenance
.
dgn-np:NP392756.RAPLOt6ykB-OfZMf0jtYSmTfQJrrYsXy12j76gtdAOn7I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP392756.RAPLOt6ykB-OfZMf0jtYSmTfQJrrYsXy12j76gtdAOn7I130_assertion
{
miriam-gene:1378
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGN9be9d648f055caf0c658b98af15ca6d1
sio:SIO_000628
miriam-gene:1378
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP392756.RAPLOt6ykB-OfZMf0jtYSmTfQJrrYsXy12j76gtdAOn7I130_provenance
{
dgn-np:NP392756.RAPLOt6ykB-OfZMf0jtYSmTfQJrrYsXy12j76gtdAOn7I130_assertion
dcterms:description
"[These included, (a) absent CR1 phenotype in a patient whose family had moderate and high CR1 numbers, (b) increasing CR1 numbers as SLE patients went into remission, (c) CR1 numbers were lower in patients with active compared with inactive disease and (d) CR1 numbers were different in each of two sets of identical twins (Fig.]. 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:2937582
;
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:NP392756.RAPLOt6ykB-OfZMf0jtYSmTfQJrrYsXy12j76gtdAOn7I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:54+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" .
}