@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP232556.RA6AGiXOeUOV769_utdUiGLZFnRTClD-MpTb1r3-y9Yg0
> .
@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:NP232556.RA6AGiXOeUOV769_utdUiGLZFnRTClD-MpTb1r3-y9Yg0130_head
{
this:
np:hasAssertion
dgn-np:NP232556.RA6AGiXOeUOV769_utdUiGLZFnRTClD-MpTb1r3-y9Yg0130_assertion
;
np:hasProvenance
dgn-np:NP232556.RA6AGiXOeUOV769_utdUiGLZFnRTClD-MpTb1r3-y9Yg0130_provenance
;
np:hasPublicationInfo
dgn-np:NP232556.RA6AGiXOeUOV769_utdUiGLZFnRTClD-MpTb1r3-y9Yg0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP232556.RA6AGiXOeUOV769_utdUiGLZFnRTClD-MpTb1r3-y9Yg0130_assertion
a
np:Assertion
.
dgn-np:NP232556.RA6AGiXOeUOV769_utdUiGLZFnRTClD-MpTb1r3-y9Yg0130_provenance
a
np:Provenance
.
dgn-np:NP232556.RA6AGiXOeUOV769_utdUiGLZFnRTClD-MpTb1r3-y9Yg0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP232556.RA6AGiXOeUOV769_utdUiGLZFnRTClD-MpTb1r3-y9Yg0130_assertion
{
miriam-gene:4488
a
ncit:C16612
.
lld:C0010278
a
ncit:C7057
.
dgn-gda:DGN771fe33da6ca042ce73c74d1af85ecf7
sio:SIO_000628
miriam-gene:4488
,
lld:C0010278
;
a
sio:SIO_001121
.
}
dgn-np:NP232556.RA6AGiXOeUOV769_utdUiGLZFnRTClD-MpTb1r3-y9Yg0130_provenance
{
dgn-np:NP232556.RA6AGiXOeUOV769_utdUiGLZFnRTClD-MpTb1r3-y9Yg0130_assertion
dcterms:description
"[The identification in craniosynostosis syndromes of mutations in genes belonging to the fibroblast growth factor signalling pathway and the transcriptional regulator MSX2 provides important clues to the pathogenesis of these disorders.]. 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:8782984
;
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:NP232556.RA6AGiXOeUOV769_utdUiGLZFnRTClD-MpTb1r3-y9Yg0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:10+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" .
}