@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP634192.RAUif4pCa6qZ61cWPU7p5xpJpWrOLNSwAg5sx3xBpvh9E
> .
@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:NP634192.RAUif4pCa6qZ61cWPU7p5xpJpWrOLNSwAg5sx3xBpvh9E130_head
{
this:
np:hasAssertion
dgn-np:NP634192.RAUif4pCa6qZ61cWPU7p5xpJpWrOLNSwAg5sx3xBpvh9E130_assertion
;
np:hasProvenance
dgn-np:NP634192.RAUif4pCa6qZ61cWPU7p5xpJpWrOLNSwAg5sx3xBpvh9E130_provenance
;
np:hasPublicationInfo
dgn-np:NP634192.RAUif4pCa6qZ61cWPU7p5xpJpWrOLNSwAg5sx3xBpvh9E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP634192.RAUif4pCa6qZ61cWPU7p5xpJpWrOLNSwAg5sx3xBpvh9E130_assertion
a
np:Assertion
.
dgn-np:NP634192.RAUif4pCa6qZ61cWPU7p5xpJpWrOLNSwAg5sx3xBpvh9E130_provenance
a
np:Provenance
.
dgn-np:NP634192.RAUif4pCa6qZ61cWPU7p5xpJpWrOLNSwAg5sx3xBpvh9E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP634192.RAUif4pCa6qZ61cWPU7p5xpJpWrOLNSwAg5sx3xBpvh9E130_assertion
{
miriam-gene:5729
a
ncit:C16612
.
lld:C0007682
a
ncit:C7057
.
dgn-gda:DGN1093337509ab5ab865b4bc2adeaada88
sio:SIO_000628
miriam-gene:5729
,
lld:C0007682
;
a
sio:SIO_001121
.
}
dgn-np:NP634192.RAUif4pCa6qZ61cWPU7p5xpJpWrOLNSwAg5sx3xBpvh9E130_provenance
{
dgn-np:NP634192.RAUif4pCa6qZ61cWPU7p5xpJpWrOLNSwAg5sx3xBpvh9E130_assertion
dcterms:description
"[Such data suggest that these alternate transcripts are involved in the molecular pathogenesis of CNS disease and perhaps in ApoE expression in general, as we show that ApoE S2 and AS1 are also transcribed in human.]. 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:16091415
;
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:NP634192.RAUif4pCa6qZ61cWPU7p5xpJpWrOLNSwAg5sx3xBpvh9E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:22+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" .
}