@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP938432.RAnSCu90alHNIkTCpqaYPpvV8nc2btq4MUYmTx1PWGQwE
> .
@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:NP938432.RAnSCu90alHNIkTCpqaYPpvV8nc2btq4MUYmTx1PWGQwE130_head
{
this:
np:hasAssertion
dgn-np:NP938432.RAnSCu90alHNIkTCpqaYPpvV8nc2btq4MUYmTx1PWGQwE130_assertion
;
np:hasProvenance
dgn-np:NP938432.RAnSCu90alHNIkTCpqaYPpvV8nc2btq4MUYmTx1PWGQwE130_provenance
;
np:hasPublicationInfo
dgn-np:NP938432.RAnSCu90alHNIkTCpqaYPpvV8nc2btq4MUYmTx1PWGQwE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP938432.RAnSCu90alHNIkTCpqaYPpvV8nc2btq4MUYmTx1PWGQwE130_assertion
a
np:Assertion
.
dgn-np:NP938432.RAnSCu90alHNIkTCpqaYPpvV8nc2btq4MUYmTx1PWGQwE130_provenance
a
np:Provenance
.
dgn-np:NP938432.RAnSCu90alHNIkTCpqaYPpvV8nc2btq4MUYmTx1PWGQwE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP938432.RAnSCu90alHNIkTCpqaYPpvV8nc2btq4MUYmTx1PWGQwE130_assertion
{
miriam-gene:64221
a
ncit:C16612
.
lld:C1846496
a
ncit:C7057
.
dgn-gda:DGNf65b896e551d00dcd010da109ee73e21
sio:SIO_000628
miriam-gene:64221
,
lld:C1846496
;
a
sio:SIO_001121
.
}
dgn-np:NP938432.RAnSCu90alHNIkTCpqaYPpvV8nc2btq4MUYmTx1PWGQwE130_provenance
{
dgn-np:NP938432.RAnSCu90alHNIkTCpqaYPpvV8nc2btq4MUYmTx1PWGQwE130_assertion
dcterms:description
"[Horizontal gaze palsy with progressive scoliosis (HGPPS) is a rare autosomal recessive disorder characterized by the absence of conjugate horizontal eye movements, and progressive scoliosis developing in childhood and adolescence, caused by mutations in the ROBO3 gene which has an important role in axonal guidance and neuronal migration.]. 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:23810770
;
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:NP938432.RAnSCu90alHNIkTCpqaYPpvV8nc2btq4MUYmTx1PWGQwE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:13+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" .
}