@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP701270.RAgI7TVHcU2dY75yjSNuElDRsBtGSCM9GO3kASNxCCFsM
> .
@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:NP701270.RAgI7TVHcU2dY75yjSNuElDRsBtGSCM9GO3kASNxCCFsM130_head
{
this:
np:hasAssertion
dgn-np:NP701270.RAgI7TVHcU2dY75yjSNuElDRsBtGSCM9GO3kASNxCCFsM130_assertion
;
np:hasProvenance
dgn-np:NP701270.RAgI7TVHcU2dY75yjSNuElDRsBtGSCM9GO3kASNxCCFsM130_provenance
;
np:hasPublicationInfo
dgn-np:NP701270.RAgI7TVHcU2dY75yjSNuElDRsBtGSCM9GO3kASNxCCFsM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP701270.RAgI7TVHcU2dY75yjSNuElDRsBtGSCM9GO3kASNxCCFsM130_assertion
a
np:Assertion
.
dgn-np:NP701270.RAgI7TVHcU2dY75yjSNuElDRsBtGSCM9GO3kASNxCCFsM130_provenance
a
np:Provenance
.
dgn-np:NP701270.RAgI7TVHcU2dY75yjSNuElDRsBtGSCM9GO3kASNxCCFsM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP701270.RAgI7TVHcU2dY75yjSNuElDRsBtGSCM9GO3kASNxCCFsM130_assertion
{
miriam-gene:2263
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNb0af683a1eb123b49ea0d2f55be51885
sio:SIO_000628
miriam-gene:2263
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP701270.RAgI7TVHcU2dY75yjSNuElDRsBtGSCM9GO3kASNxCCFsM130_provenance
{
dgn-np:NP701270.RAgI7TVHcU2dY75yjSNuElDRsBtGSCM9GO3kASNxCCFsM130_assertion
dcterms:description
"[These observations in association with the changes in FGF gene expression and in the FGF receptor number, suggest that cellular mechanisms downstream from FGF receptor binding are involved in the two different forms of AD.]. 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:17660861
;
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:NP701270.RAgI7TVHcU2dY75yjSNuElDRsBtGSCM9GO3kASNxCCFsM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:06+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" .
}