@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP712669.RA0lbXsw3rTuOsOqW3PJgvYJ0CNHB6IFNtLHziEcksedw
> .
@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:NP712669.RA0lbXsw3rTuOsOqW3PJgvYJ0CNHB6IFNtLHziEcksedw130_head
{
this:
np:hasAssertion
dgn-np:NP712669.RA0lbXsw3rTuOsOqW3PJgvYJ0CNHB6IFNtLHziEcksedw130_assertion
;
np:hasProvenance
dgn-np:NP712669.RA0lbXsw3rTuOsOqW3PJgvYJ0CNHB6IFNtLHziEcksedw130_provenance
;
np:hasPublicationInfo
dgn-np:NP712669.RA0lbXsw3rTuOsOqW3PJgvYJ0CNHB6IFNtLHziEcksedw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP712669.RA0lbXsw3rTuOsOqW3PJgvYJ0CNHB6IFNtLHziEcksedw130_assertion
a
np:Assertion
.
dgn-np:NP712669.RA0lbXsw3rTuOsOqW3PJgvYJ0CNHB6IFNtLHziEcksedw130_provenance
a
np:Provenance
.
dgn-np:NP712669.RA0lbXsw3rTuOsOqW3PJgvYJ0CNHB6IFNtLHziEcksedw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP712669.RA0lbXsw3rTuOsOqW3PJgvYJ0CNHB6IFNtLHziEcksedw130_assertion
{
miriam-gene:10046
a
ncit:C16612
.
lld:C1691215
a
ncit:C7057
.
dgn-gda:DGNd8a53d6e5877097a52a09939273df00a
sio:SIO_000628
miriam-gene:10046
,
lld:C1691215
;
a
sio:SIO_001121
.
}
dgn-np:NP712669.RA0lbXsw3rTuOsOqW3PJgvYJ0CNHB6IFNtLHziEcksedw130_provenance
{
dgn-np:NP712669.RA0lbXsw3rTuOsOqW3PJgvYJ0CNHB6IFNtLHziEcksedw130_assertion
dcterms:description
"[These findings suggest that the CXorf6 mutations cause hypospadias primarily because of testicular dysfunction and resultant compromised testosterone production around that period, and provide useful information for the molecular network involved in fetal testosterone production.]. 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:18987498
;
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:NP712669.RA0lbXsw3rTuOsOqW3PJgvYJ0CNHB6IFNtLHziEcksedw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:13+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" .
}