@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP461407.RA-QbYmfIq9wfmc-fgRjcjEyl_kCWlwtLdE8bOXttBkhw
> .
@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:NP461407.RA-QbYmfIq9wfmc-fgRjcjEyl_kCWlwtLdE8bOXttBkhw130_head
{
this:
np:hasAssertion
dgn-np:NP461407.RA-QbYmfIq9wfmc-fgRjcjEyl_kCWlwtLdE8bOXttBkhw130_assertion
;
np:hasProvenance
dgn-np:NP461407.RA-QbYmfIq9wfmc-fgRjcjEyl_kCWlwtLdE8bOXttBkhw130_provenance
;
np:hasPublicationInfo
dgn-np:NP461407.RA-QbYmfIq9wfmc-fgRjcjEyl_kCWlwtLdE8bOXttBkhw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP461407.RA-QbYmfIq9wfmc-fgRjcjEyl_kCWlwtLdE8bOXttBkhw130_assertion
a
np:Assertion
.
dgn-np:NP461407.RA-QbYmfIq9wfmc-fgRjcjEyl_kCWlwtLdE8bOXttBkhw130_provenance
a
np:Provenance
.
dgn-np:NP461407.RA-QbYmfIq9wfmc-fgRjcjEyl_kCWlwtLdE8bOXttBkhw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP461407.RA-QbYmfIq9wfmc-fgRjcjEyl_kCWlwtLdE8bOXttBkhw130_assertion
{
miriam-gene:2296
a
ncit:C16612
.
lld:C3495488
a
ncit:C7057
.
dgn-gda:DGNd6db6e5629abc37f372815111b17571e
sio:SIO_000628
miriam-gene:2296
,
lld:C3495488
;
a
sio:SIO_001121
.
}
dgn-np:NP461407.RA-QbYmfIq9wfmc-fgRjcjEyl_kCWlwtLdE8bOXttBkhw130_provenance
{
dgn-np:NP461407.RA-QbYmfIq9wfmc-fgRjcjEyl_kCWlwtLdE8bOXttBkhw130_assertion
dcterms:description
"[We suggest that this FOXC1 mutation causes typical ARS, and that our results may be useful for better understanding of the spectrum of FOXC1 mutations and the role of FOXC1 in the development and progression of ARS.]. 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:23687430
;
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:NP461407.RA-QbYmfIq9wfmc-fgRjcjEyl_kCWlwtLdE8bOXttBkhw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:34+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" .
}