@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP830793.RAGd5_ZB9sIbkGXS6HF3SjeavJMAe66OSjo9Rxp5ssRaI
> .
@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:NP830793.RAGd5_ZB9sIbkGXS6HF3SjeavJMAe66OSjo9Rxp5ssRaI130_head
{
this:
np:hasAssertion
dgn-np:NP830793.RAGd5_ZB9sIbkGXS6HF3SjeavJMAe66OSjo9Rxp5ssRaI130_assertion
;
np:hasProvenance
dgn-np:NP830793.RAGd5_ZB9sIbkGXS6HF3SjeavJMAe66OSjo9Rxp5ssRaI130_provenance
;
np:hasPublicationInfo
dgn-np:NP830793.RAGd5_ZB9sIbkGXS6HF3SjeavJMAe66OSjo9Rxp5ssRaI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP830793.RAGd5_ZB9sIbkGXS6HF3SjeavJMAe66OSjo9Rxp5ssRaI130_assertion
a
np:Assertion
.
dgn-np:NP830793.RAGd5_ZB9sIbkGXS6HF3SjeavJMAe66OSjo9Rxp5ssRaI130_provenance
a
np:Provenance
.
dgn-np:NP830793.RAGd5_ZB9sIbkGXS6HF3SjeavJMAe66OSjo9Rxp5ssRaI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP830793.RAGd5_ZB9sIbkGXS6HF3SjeavJMAe66OSjo9Rxp5ssRaI130_assertion
{
miriam-gene:6736
a
ncit:C16612
.
lld:C0018055
a
ncit:C7057
.
dgn-gda:DGN4e259b35ceb28828aa23d48963662268
sio:SIO_000628
miriam-gene:6736
,
lld:C0018055
;
a
sio:SIO_001121
.
}
dgn-np:NP830793.RAGd5_ZB9sIbkGXS6HF3SjeavJMAe66OSjo9Rxp5ssRaI130_provenance
{
dgn-np:NP830793.RAGd5_ZB9sIbkGXS6HF3SjeavJMAe66OSjo9Rxp5ssRaI130_assertion
dcterms:description
"[While mosaicism alone might have accounted for the phenotypic differences, by PCR analysis the Turner syndrome patient was SRY and ZFY negative and the mixed gonadal dysgenesis patient was SRY and ZFY positive.]. 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:9783714
;
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:NP830793.RAGd5_ZB9sIbkGXS6HF3SjeavJMAe66OSjo9Rxp5ssRaI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:28+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" .
}