@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP767660.RA2GlhC-iGB-brTPWq4kKmQPyqMMkMW3DNsljICo6iQr0
> .
@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:NP767660.RA2GlhC-iGB-brTPWq4kKmQPyqMMkMW3DNsljICo6iQr0130_head
{
this:
np:hasAssertion
dgn-np:NP767660.RA2GlhC-iGB-brTPWq4kKmQPyqMMkMW3DNsljICo6iQr0130_assertion
;
np:hasProvenance
dgn-np:NP767660.RA2GlhC-iGB-brTPWq4kKmQPyqMMkMW3DNsljICo6iQr0130_provenance
;
np:hasPublicationInfo
dgn-np:NP767660.RA2GlhC-iGB-brTPWq4kKmQPyqMMkMW3DNsljICo6iQr0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP767660.RA2GlhC-iGB-brTPWq4kKmQPyqMMkMW3DNsljICo6iQr0130_assertion
a
np:Assertion
.
dgn-np:NP767660.RA2GlhC-iGB-brTPWq4kKmQPyqMMkMW3DNsljICo6iQr0130_provenance
a
np:Provenance
.
dgn-np:NP767660.RA2GlhC-iGB-brTPWq4kKmQPyqMMkMW3DNsljICo6iQr0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP767660.RA2GlhC-iGB-brTPWq4kKmQPyqMMkMW3DNsljICo6iQr0130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0010417
a
ncit:C7057
.
dgn-gda:DGN49848d0eee3962bd693697747ac580ba
sio:SIO_000628
miriam-gene:367
,
lld:C0010417
;
a
sio:SIO_001121
.
}
dgn-np:NP767660.RA2GlhC-iGB-brTPWq4kKmQPyqMMkMW3DNsljICo6iQr0130_provenance
{
dgn-np:NP767660.RA2GlhC-iGB-brTPWq4kKmQPyqMMkMW3DNsljICo6iQr0130_assertion
dcterms:description
"[Mutations in the gene for insulin-like factor 3 and its receptor and in the androgen receptor gene have been recognized as causes of cryptorchidism in some cases, but some chromosomal alterations, above all the Klinefelter syndrome, are also frequently involved.]. 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:18436703
;
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:NP767660.RA2GlhC-iGB-brTPWq4kKmQPyqMMkMW3DNsljICo6iQr0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:44+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" .
}