@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP717655.RA69qJALRscvEM4cI3j29x0FPjSoySSs1QseYh_8Plcbw
> .
@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:NP717655.RA69qJALRscvEM4cI3j29x0FPjSoySSs1QseYh_8Plcbw130_head
{
this:
np:hasAssertion
dgn-np:NP717655.RA69qJALRscvEM4cI3j29x0FPjSoySSs1QseYh_8Plcbw130_assertion
;
np:hasProvenance
dgn-np:NP717655.RA69qJALRscvEM4cI3j29x0FPjSoySSs1QseYh_8Plcbw130_provenance
;
np:hasPublicationInfo
dgn-np:NP717655.RA69qJALRscvEM4cI3j29x0FPjSoySSs1QseYh_8Plcbw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP717655.RA69qJALRscvEM4cI3j29x0FPjSoySSs1QseYh_8Plcbw130_assertion
a
np:Assertion
.
dgn-np:NP717655.RA69qJALRscvEM4cI3j29x0FPjSoySSs1QseYh_8Plcbw130_provenance
a
np:Provenance
.
dgn-np:NP717655.RA69qJALRscvEM4cI3j29x0FPjSoySSs1QseYh_8Plcbw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP717655.RA69qJALRscvEM4cI3j29x0FPjSoySSs1QseYh_8Plcbw130_assertion
{
miriam-gene:2516
a
ncit:C16612
.
lld:C1261504
a
ncit:C7057
.
dgn-gda:DGNc3e80d2d47ca1a6c6a0179f878be1abb
sio:SIO_000628
miriam-gene:2516
,
lld:C1261504
;
a
sio:SIO_001121
.
}
dgn-np:NP717655.RA69qJALRscvEM4cI3j29x0FPjSoySSs1QseYh_8Plcbw130_provenance
{
dgn-np:NP717655.RA69qJALRscvEM4cI3j29x0FPjSoySSs1QseYh_8Plcbw130_assertion
dcterms:description
"[METHODS This study involved mutational analysis of NR5A1 in 24 individuals with bilateral anorchia and micropenis from the French Collaborative Anorchia study, as well as in vitro functional studies of SF1-dependent transcriptional activation and computer modeling.]. 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:17940071
;
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:NP717655.RA69qJALRscvEM4cI3j29x0FPjSoySSs1QseYh_8Plcbw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:16+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" .
}