@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP398204.RAl8STTch799qQINaim-SQQmZRKmU4MocPfhXl1wf9bcs
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP398204.RAl8STTch799qQINaim-SQQmZRKmU4MocPfhXl1wf9bcs130_head
{
this:
np:hasAssertion
dgn-np:NP398204.RAl8STTch799qQINaim-SQQmZRKmU4MocPfhXl1wf9bcs130_assertion
;
np:hasProvenance
dgn-np:NP398204.RAl8STTch799qQINaim-SQQmZRKmU4MocPfhXl1wf9bcs130_provenance
;
np:hasPublicationInfo
dgn-np:NP398204.RAl8STTch799qQINaim-SQQmZRKmU4MocPfhXl1wf9bcs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP398204.RAl8STTch799qQINaim-SQQmZRKmU4MocPfhXl1wf9bcs130_assertion
a
np:Assertion
.
dgn-np:NP398204.RAl8STTch799qQINaim-SQQmZRKmU4MocPfhXl1wf9bcs130_provenance
a
np:Provenance
.
dgn-np:NP398204.RAl8STTch799qQINaim-SQQmZRKmU4MocPfhXl1wf9bcs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP398204.RAl8STTch799qQINaim-SQQmZRKmU4MocPfhXl1wf9bcs130_assertion
{
miriam-gene:2246
a
ncit:C16612
.
lld:C0149521
a
ncit:C7057
.
dgn-gda:DGN1a1221efd2688ce030a88d38c0e10cbe
sio:SIO_000628
miriam-gene:2246
,
lld:C0149521
;
a
sio:SIO_001121
.
}
dgn-np:NP398204.RAl8STTch799qQINaim-SQQmZRKmU4MocPfhXl1wf9bcs130_provenance
{
dgn-np:NP398204.RAl8STTch799qQINaim-SQQmZRKmU4MocPfhXl1wf9bcs130_assertion
dcterms:description
"[These findings suggest that aFGF and bFGF may either be involved in the pathobiological mechanisms that occur in CP, or that their overexpression may be the consequence of other perturbations that occur in this disorder.]. 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:7507297
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP398204.RAl8STTch799qQINaim-SQQmZRKmU4MocPfhXl1wf9bcs130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:31+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}