@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP679078.RALpRRO-EF98OvFSgI5OMNt_slJfEMezlBmmRaLJmCDos
> .
@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:NP679078.RALpRRO-EF98OvFSgI5OMNt_slJfEMezlBmmRaLJmCDos130_head
{
this:
np:hasAssertion
dgn-np:NP679078.RALpRRO-EF98OvFSgI5OMNt_slJfEMezlBmmRaLJmCDos130_assertion
;
np:hasProvenance
dgn-np:NP679078.RALpRRO-EF98OvFSgI5OMNt_slJfEMezlBmmRaLJmCDos130_provenance
;
np:hasPublicationInfo
dgn-np:NP679078.RALpRRO-EF98OvFSgI5OMNt_slJfEMezlBmmRaLJmCDos130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP679078.RALpRRO-EF98OvFSgI5OMNt_slJfEMezlBmmRaLJmCDos130_assertion
a
np:Assertion
.
dgn-np:NP679078.RALpRRO-EF98OvFSgI5OMNt_slJfEMezlBmmRaLJmCDos130_provenance
a
np:Provenance
.
dgn-np:NP679078.RALpRRO-EF98OvFSgI5OMNt_slJfEMezlBmmRaLJmCDos130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP679078.RALpRRO-EF98OvFSgI5OMNt_slJfEMezlBmmRaLJmCDos130_assertion
{
miriam-gene:122042
a
ncit:C16612
.
lld:C0021359
a
ncit:C7057
.
dgn-gda:DGN41c4ec8522ef4acbf52be38e9ac775e9
sio:SIO_000628
miriam-gene:122042
,
lld:C0021359
;
a
sio:SIO_001121
.
}
dgn-np:NP679078.RALpRRO-EF98OvFSgI5OMNt_slJfEMezlBmmRaLJmCDos130_provenance
{
dgn-np:NP679078.RALpRRO-EF98OvFSgI5OMNt_slJfEMezlBmmRaLJmCDos130_assertion
dcterms:description
"[Although a role for mutations of INSL3 and LGR8 genes in cryptorchidism is reasonable, additional studies are needed to establish an association between the disruption of INSL3 pathway and higher risk of infertility or testicular cancer.]. 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:16687567
;
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:NP679078.RALpRRO-EF98OvFSgI5OMNt_slJfEMezlBmmRaLJmCDos130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:49+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" .
}