@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk
> .
@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:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_head
{
this:
np:hasAssertion
dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_assertion
;
np:hasProvenance
dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_provenance
;
np:hasPublicationInfo
dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_assertion
a
np:Assertion
.
dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_provenance
a
np:Provenance
.
dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_assertion
{
miriam-gene:650
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGN18a1823c343f4fffb36238d8ed87c131
sio:SIO_000628
miriam-gene:650
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_provenance
{
dgn-np:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_assertion
dcterms:description
"[The abundance of neural stem cells (NSCs) in multiple sclerosis (MS) lesions with extensive astrogliosis suggests that fate factors of NSCs, such as the bone morphogenic protein (BMP) signaling maybe defective in MS. We found an elevated mRNA expression and protein secretion of BMP-2,4,5 but not of BMP-7.]. 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:24080309
;
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:NP154363.RA7vt0MMU0F6JBOsK5c2ONhhBeiMkAAs3fX7Kbr4A-lLk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:22+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" .
}