@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE
> .
@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:NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_head
{
this:
np:hasAssertion
dgn-np:NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_assertion
;
np:hasProvenance
dgn-np:NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_provenance
;
np:hasPublicationInfo
dgn-np:NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_assertion
a
np:Assertion
.
dgn-np:NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_provenance
a
np:Provenance
.
dgn-np:NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_assertion
{
miriam-gene:3640
a
ncit:C16612
.
lld:C0010417
a
ncit:C7057
.
dgn-gda:DGN6dd8ac5a5d5e9ddfd074ca3fa1c315d5
sio:SIO_000628
miriam-gene:3640
,
lld:C0010417
;
a
sio:SIO_001121
.
}
dgn-np:NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_provenance
{
dgn-np:NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_assertion
dcterms:description
"[Although some cases of isolated cryptorchidism in humans can be ascribed to known genetic defects, such as mutations in INSL3 or RXFP2, the cause of cryptorchidism remains unknown in most patients.]. 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:21403659
;
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:NP267368.RAnGUklypT2ZNxGq4ihkLoE59Kgqp5fSACkn6NJ9YDyPE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:29+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" .
}