@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk
> .
@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:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_head
{
this:
np:hasAssertion
dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_assertion
;
np:hasProvenance
dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_provenance
;
np:hasPublicationInfo
dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_assertion
a
np:Assertion
.
dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_provenance
a
np:Provenance
.
dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_assertion
{
miriam-gene:7422
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN0cd010da5ed41c3da843a8354e6d9d4e
sio:SIO_000628
miriam-gene:7422
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_provenance
{
dgn-np:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_assertion
dcterms:description
"[Although VEGF gene expression is mainly stimulated by hypoxia, we have measured lower VEGF levels in cerebrospinal fluid (CSF) from hypoxaemic patients with amyotrophic lateral sclerosis (ALS) than in CSF from normoxaemic patients with 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:16421133
;
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:NP182179.RAtl_9oZN1u4blkKAWmO-DUOttC-llWE3SqdjW-LnUkVk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:38+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" .
}