@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP787324.RA3jLbjop9FfCRszLGXnDsUCTd_byQfhRw53dV4oE0YGQ
> .
@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:NP787324.RA3jLbjop9FfCRszLGXnDsUCTd_byQfhRw53dV4oE0YGQ130_head
{
this:
np:hasAssertion
dgn-np:NP787324.RA3jLbjop9FfCRszLGXnDsUCTd_byQfhRw53dV4oE0YGQ130_assertion
;
np:hasProvenance
dgn-np:NP787324.RA3jLbjop9FfCRszLGXnDsUCTd_byQfhRw53dV4oE0YGQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP787324.RA3jLbjop9FfCRszLGXnDsUCTd_byQfhRw53dV4oE0YGQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP787324.RA3jLbjop9FfCRszLGXnDsUCTd_byQfhRw53dV4oE0YGQ130_assertion
a
np:Assertion
.
dgn-np:NP787324.RA3jLbjop9FfCRszLGXnDsUCTd_byQfhRw53dV4oE0YGQ130_provenance
a
np:Provenance
.
dgn-np:NP787324.RA3jLbjop9FfCRszLGXnDsUCTd_byQfhRw53dV4oE0YGQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP787324.RA3jLbjop9FfCRszLGXnDsUCTd_byQfhRw53dV4oE0YGQ130_assertion
{
miriam-gene:3640
a
ncit:C16612
.
lld:C0431663
a
ncit:C7057
.
dgn-gda:DGN3324fbf36f4354f16228240cf18fd1a7
sio:SIO_000628
miriam-gene:3640
,
lld:C0431663
;
a
sio:SIO_001121
.
}
dgn-np:NP787324.RA3jLbjop9FfCRszLGXnDsUCTd_byQfhRw53dV4oE0YGQ130_provenance
{
dgn-np:NP787324.RA3jLbjop9FfCRszLGXnDsUCTd_byQfhRw53dV4oE0YGQ130_assertion
dcterms:description
"[Recently, the absence of the Insl3 gene has been reported to result in bilateral cryptorchidism in male mice and it has been suggested that mutations of the INSL3 gene may cause cryptorchidism in humans.]. 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:11380919
;
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:NP787324.RA3jLbjop9FfCRszLGXnDsUCTd_byQfhRw53dV4oE0YGQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:00+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" .
}