@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP216409.RAiUyg3C5DDcwqZvfJZJp5UOcQMZDoByCI9wa3Ht2Gp5I
> .
@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:NP216409.RAiUyg3C5DDcwqZvfJZJp5UOcQMZDoByCI9wa3Ht2Gp5I130_head
{
this:
np:hasAssertion
dgn-np:NP216409.RAiUyg3C5DDcwqZvfJZJp5UOcQMZDoByCI9wa3Ht2Gp5I130_assertion
;
np:hasProvenance
dgn-np:NP216409.RAiUyg3C5DDcwqZvfJZJp5UOcQMZDoByCI9wa3Ht2Gp5I130_provenance
;
np:hasPublicationInfo
dgn-np:NP216409.RAiUyg3C5DDcwqZvfJZJp5UOcQMZDoByCI9wa3Ht2Gp5I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP216409.RAiUyg3C5DDcwqZvfJZJp5UOcQMZDoByCI9wa3Ht2Gp5I130_assertion
a
np:Assertion
.
dgn-np:NP216409.RAiUyg3C5DDcwqZvfJZJp5UOcQMZDoByCI9wa3Ht2Gp5I130_provenance
a
np:Provenance
.
dgn-np:NP216409.RAiUyg3C5DDcwqZvfJZJp5UOcQMZDoByCI9wa3Ht2Gp5I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP216409.RAiUyg3C5DDcwqZvfJZJp5UOcQMZDoByCI9wa3Ht2Gp5I130_assertion
{
miriam-gene:7291
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN2b88615d34e224e9b73e6f2364d65491
sio:SIO_000628
miriam-gene:7291
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP216409.RAiUyg3C5DDcwqZvfJZJp5UOcQMZDoByCI9wa3Ht2Gp5I130_provenance
{
dgn-np:NP216409.RAiUyg3C5DDcwqZvfJZJp5UOcQMZDoByCI9wa3Ht2Gp5I130_assertion
dcterms:description
"[Our data confirm that fibroblast growth factor signalling pathways are involved in craniofacial development and suggest that some human malformation pedigrees or sporadic craniosynostosis may be caused by mutations that deregulate expression of the Fgf ligands.]. 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:9626498
;
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:NP216409.RAiUyg3C5DDcwqZvfJZJp5UOcQMZDoByCI9wa3Ht2Gp5I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+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" .
}