@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_assertion
;
np:hasProvenance
dgn-np:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_provenance
;
np:hasPublicationInfo
dgn-np:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_assertion
a
np:Assertion
.
dgn-np:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_provenance
a
np:Provenance
.
dgn-np:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_assertion
{
miriam-gene:54209
a
ncit:C16612
.
lld:C1857316
a
ncit:C7057
.
dgn-gda:DGN2613b2098f9ee80878bc85c968825927
sio:SIO_000628
miriam-gene:54209
,
lld:C1857316
;
a
sio:SIO_001121
.
}
dgn-np:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_provenance
{
dgn-np:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_assertion
dcterms:description
"[In this paper, we have studied polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLOSL), an early onset dementia with bone fractures caused by mutations in TYROBP (DAP12) and TREM2 genes, which encode important signaling molecules in human dendritic cells (DCs).]. 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:17530208
;
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:NP693535.RAcps3OE3xdC2Ap6TDWuvBtDWmh1sbn7pMwpAQ-nJlyZw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:01+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
<
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> , <
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" .
}