@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc
> .
@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:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_head
{
this:
np:hasAssertion
dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_assertion
;
np:hasProvenance
dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_provenance
;
np:hasPublicationInfo
dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_assertion
a
np:Assertion
.
dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_provenance
a
np:Provenance
.
dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_assertion
{
miriam-gene:2253
a
ncit:C16612
.
lld:C0206718
a
ncit:C7057
.
dgn-gda:DGNd816489f97b3046155c9c1a35ad337d9
sio:SIO_000628
miriam-gene:2253
,
lld:C0206718
;
a
sio:SIO_001121
.
}
dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_provenance
{
dgn-np:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_assertion
dcterms:description
"[In accordance with these in vitro findings, the immunohistochemical analysis on human neurological diseases showed that FGF8 expression is evident in differentiating histological types of neuroblastoma and ganglioneuroblastoma, and that the levels of FGF8 immunoreactivity in the substantia nigra from Parkinson's disease are significantly lower than those in age-matched controls.]. 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:11532426
;
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:NP764461.RAON2Ui7NejBYA2Zc-rg3UpwXiAY-L2psRaqOOkuvDqpc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:42+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" .
}