@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg
> .
@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:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_head
{
this:
np:hasAssertion
dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_assertion
;
np:hasProvenance
dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_provenance
;
np:hasPublicationInfo
dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_assertion
a
np:Assertion
.
dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_provenance
a
np:Provenance
.
dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_assertion
{
miriam-gene:6736
a
ncit:C16612
.
lld:C0042755
a
ncit:C7057
.
dgn-gda:DGN3c13186251573ac33016743fa9b11f09
sio:SIO_000628
miriam-gene:6736
,
lld:C0042755
;
a
sio:SIO_001121
.
}
dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_provenance
{
dgn-np:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_assertion
dcterms:description
"[In this study, five very rare cases of SRY carrying subjects (two XX males and three XX true hermaphrodites) with various degrees of incomplete masculinisation were analysed in order to elucidate the cause of sexual ambiguity despite the presence of the SRY gene.]. 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:10874632
;
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:NP478095.RAA-aK9aTp2dYeviw6kZ0lCciOZqdPtLCdqem31JPa-Mg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:46+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" .
}