@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP293936.RAvmYhaRtAT6HZrQY5ITSnhRVKPcynhsvvDeJf4dSo2yY
> .
@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:NP293936.RAvmYhaRtAT6HZrQY5ITSnhRVKPcynhsvvDeJf4dSo2yY130_head
{
this:
np:hasAssertion
dgn-np:NP293936.RAvmYhaRtAT6HZrQY5ITSnhRVKPcynhsvvDeJf4dSo2yY130_assertion
;
np:hasProvenance
dgn-np:NP293936.RAvmYhaRtAT6HZrQY5ITSnhRVKPcynhsvvDeJf4dSo2yY130_provenance
;
np:hasPublicationInfo
dgn-np:NP293936.RAvmYhaRtAT6HZrQY5ITSnhRVKPcynhsvvDeJf4dSo2yY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP293936.RAvmYhaRtAT6HZrQY5ITSnhRVKPcynhsvvDeJf4dSo2yY130_assertion
a
np:Assertion
.
dgn-np:NP293936.RAvmYhaRtAT6HZrQY5ITSnhRVKPcynhsvvDeJf4dSo2yY130_provenance
a
np:Provenance
.
dgn-np:NP293936.RAvmYhaRtAT6HZrQY5ITSnhRVKPcynhsvvDeJf4dSo2yY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP293936.RAvmYhaRtAT6HZrQY5ITSnhRVKPcynhsvvDeJf4dSo2yY130_assertion
{
miriam-gene:412
a
ncit:C16612
.
lld:C2717836
a
ncit:C7057
.
dgn-gda:DGN581317dad900b3690fe6ea7193544aec
sio:SIO_000628
miriam-gene:412
,
lld:C2717836
;
a
sio:SIO_001121
.
}
dgn-np:NP293936.RAvmYhaRtAT6HZrQY5ITSnhRVKPcynhsvvDeJf4dSo2yY130_provenance
{
dgn-np:NP293936.RAvmYhaRtAT6HZrQY5ITSnhRVKPcynhsvvDeJf4dSo2yY130_assertion
dcterms:description
"[To ascertain all prenatally diagnosed cases of Steroid Sulfatase (STS) deficiency in British Columbia between August 2002 and July 2007 to determine the incidence of this condition, the clinical and laboratory findings, and the risk of a contiguous gene deletion syndrome.]. 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:19609942
;
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:NP293936.RAvmYhaRtAT6HZrQY5ITSnhRVKPcynhsvvDeJf4dSo2yY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:47+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" .
}