@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP352232.RAwA3GiTGcdmL6d7yQJbi0dWeQT9xGLUfimee3GAAVJXM
> .
@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:NP352232.RAwA3GiTGcdmL6d7yQJbi0dWeQT9xGLUfimee3GAAVJXM130_head
{
this:
np:hasAssertion
dgn-np:NP352232.RAwA3GiTGcdmL6d7yQJbi0dWeQT9xGLUfimee3GAAVJXM130_assertion
;
np:hasProvenance
dgn-np:NP352232.RAwA3GiTGcdmL6d7yQJbi0dWeQT9xGLUfimee3GAAVJXM130_provenance
;
np:hasPublicationInfo
dgn-np:NP352232.RAwA3GiTGcdmL6d7yQJbi0dWeQT9xGLUfimee3GAAVJXM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP352232.RAwA3GiTGcdmL6d7yQJbi0dWeQT9xGLUfimee3GAAVJXM130_assertion
a
np:Assertion
.
dgn-np:NP352232.RAwA3GiTGcdmL6d7yQJbi0dWeQT9xGLUfimee3GAAVJXM130_provenance
a
np:Provenance
.
dgn-np:NP352232.RAwA3GiTGcdmL6d7yQJbi0dWeQT9xGLUfimee3GAAVJXM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP352232.RAwA3GiTGcdmL6d7yQJbi0dWeQT9xGLUfimee3GAAVJXM130_assertion
{
miriam-gene:3791
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN33d7c3bc315d12004d476782c1a0f9ec
sio:SIO_000628
miriam-gene:3791
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP352232.RAwA3GiTGcdmL6d7yQJbi0dWeQT9xGLUfimee3GAAVJXM130_provenance
{
dgn-np:NP352232.RAwA3GiTGcdmL6d7yQJbi0dWeQT9xGLUfimee3GAAVJXM130_assertion
dcterms:description
"[The similar expression patterns of VEGF and VEGFR2 suggests autocrine/paracrine effects on spinal motor neurons, and the reduction in their expression seen in ALS cases would support the hypothesis that, as in mouse models of the disease, reduced VEGF signaling may play a role in the pathogenesis of ALS.]. 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:16410746
;
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:NP352232.RAwA3GiTGcdmL6d7yQJbi0dWeQT9xGLUfimee3GAAVJXM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:27+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" .
}