@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP236564.RAvR18dWVkhEz6b57DD4OIDwGCL3pyGOqpxgeA2rAasBk
> .
@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:NP236564.RAvR18dWVkhEz6b57DD4OIDwGCL3pyGOqpxgeA2rAasBk130_head
{
this:
np:hasAssertion
dgn-np:NP236564.RAvR18dWVkhEz6b57DD4OIDwGCL3pyGOqpxgeA2rAasBk130_assertion
;
np:hasProvenance
dgn-np:NP236564.RAvR18dWVkhEz6b57DD4OIDwGCL3pyGOqpxgeA2rAasBk130_provenance
;
np:hasPublicationInfo
dgn-np:NP236564.RAvR18dWVkhEz6b57DD4OIDwGCL3pyGOqpxgeA2rAasBk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP236564.RAvR18dWVkhEz6b57DD4OIDwGCL3pyGOqpxgeA2rAasBk130_assertion
a
np:Assertion
.
dgn-np:NP236564.RAvR18dWVkhEz6b57DD4OIDwGCL3pyGOqpxgeA2rAasBk130_provenance
a
np:Provenance
.
dgn-np:NP236564.RAvR18dWVkhEz6b57DD4OIDwGCL3pyGOqpxgeA2rAasBk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP236564.RAvR18dWVkhEz6b57DD4OIDwGCL3pyGOqpxgeA2rAasBk130_assertion
{
miriam-gene:6736
a
ncit:C16612
.
lld:C0018051
a
ncit:C7057
.
dgn-gda:DGNbf81d53b186ad399dc566bf9201ac582
sio:SIO_000628
miriam-gene:6736
,
lld:C0018051
;
a
sio:SIO_001121
.
}
dgn-np:NP236564.RAvR18dWVkhEz6b57DD4OIDwGCL3pyGOqpxgeA2rAasBk130_provenance
{
dgn-np:NP236564.RAvR18dWVkhEz6b57DD4OIDwGCL3pyGOqpxgeA2rAasBk130_assertion
dcterms:description
"[Gonadal dysgenesis may be isolated, as in the case of SRY mutations, or associated with abnormal development of other organs, such as bone or adrenals, consistent with the spatial expression profile of the disrupted genes (SOX9 or SF1).]. 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:11990797
;
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:NP236564.RAvR18dWVkhEz6b57DD4OIDwGCL3pyGOqpxgeA2rAasBk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:12+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" .
}