@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP172122.RAs_MnMNURlk-FLIcTVZRPMh1scy_kXvKPZ9xJY6UmGuI
> .
@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:NP172122.RAs_MnMNURlk-FLIcTVZRPMh1scy_kXvKPZ9xJY6UmGuI130_head
{
this:
np:hasAssertion
dgn-np:NP172122.RAs_MnMNURlk-FLIcTVZRPMh1scy_kXvKPZ9xJY6UmGuI130_assertion
;
np:hasProvenance
dgn-np:NP172122.RAs_MnMNURlk-FLIcTVZRPMh1scy_kXvKPZ9xJY6UmGuI130_provenance
;
np:hasPublicationInfo
dgn-np:NP172122.RAs_MnMNURlk-FLIcTVZRPMh1scy_kXvKPZ9xJY6UmGuI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP172122.RAs_MnMNURlk-FLIcTVZRPMh1scy_kXvKPZ9xJY6UmGuI130_assertion
a
np:Assertion
.
dgn-np:NP172122.RAs_MnMNURlk-FLIcTVZRPMh1scy_kXvKPZ9xJY6UmGuI130_provenance
a
np:Provenance
.
dgn-np:NP172122.RAs_MnMNURlk-FLIcTVZRPMh1scy_kXvKPZ9xJY6UmGuI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP172122.RAs_MnMNURlk-FLIcTVZRPMh1scy_kXvKPZ9xJY6UmGuI130_assertion
{
miriam-gene:6736
a
ncit:C16612
.
lld:C0553573
a
ncit:C7057
.
dgn-gda:DGN557c766d56fbda8f58b35617a4335a8b
sio:SIO_000628
miriam-gene:6736
,
lld:C0553573
;
a
sio:SIO_001121
.
}
dgn-np:NP172122.RAs_MnMNURlk-FLIcTVZRPMh1scy_kXvKPZ9xJY6UmGuI130_provenance
{
dgn-np:NP172122.RAs_MnMNURlk-FLIcTVZRPMh1scy_kXvKPZ9xJY6UmGuI130_assertion
dcterms:description
"[Our results suggest that lack of a second sex chromosome in majority cells of the patient may have triggered the short stature and primary infertility, and the mutated SRY protein may be associated with the development of gonadoblastoma.]. 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:20849656
;
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:NP172122.RAs_MnMNURlk-FLIcTVZRPMh1scy_kXvKPZ9xJY6UmGuI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:33+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" .
}