@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP469509.RAwlHDqb0LJ5QKtPjdMhzIyogwAubUOr1iIybQa5HRiHk
> .
@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:NP469509.RAwlHDqb0LJ5QKtPjdMhzIyogwAubUOr1iIybQa5HRiHk130_head
{
this:
np:hasAssertion
dgn-np:NP469509.RAwlHDqb0LJ5QKtPjdMhzIyogwAubUOr1iIybQa5HRiHk130_assertion
;
np:hasProvenance
dgn-np:NP469509.RAwlHDqb0LJ5QKtPjdMhzIyogwAubUOr1iIybQa5HRiHk130_provenance
;
np:hasPublicationInfo
dgn-np:NP469509.RAwlHDqb0LJ5QKtPjdMhzIyogwAubUOr1iIybQa5HRiHk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP469509.RAwlHDqb0LJ5QKtPjdMhzIyogwAubUOr1iIybQa5HRiHk130_assertion
a
np:Assertion
.
dgn-np:NP469509.RAwlHDqb0LJ5QKtPjdMhzIyogwAubUOr1iIybQa5HRiHk130_provenance
a
np:Provenance
.
dgn-np:NP469509.RAwlHDqb0LJ5QKtPjdMhzIyogwAubUOr1iIybQa5HRiHk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP469509.RAwlHDqb0LJ5QKtPjdMhzIyogwAubUOr1iIybQa5HRiHk130_assertion
{
miriam-gene:4863
a
ncit:C16612
.
lld:C1691215
a
ncit:C7057
.
dgn-gda:DGNcc28ffd6e254aafd2f5556f132c0359f
sio:SIO_000628
miriam-gene:4863
,
lld:C1691215
;
a
sio:SIO_001121
.
}
dgn-np:NP469509.RAwlHDqb0LJ5QKtPjdMhzIyogwAubUOr1iIybQa5HRiHk130_provenance
{
dgn-np:NP469509.RAwlHDqb0LJ5QKtPjdMhzIyogwAubUOr1iIybQa5HRiHk130_assertion
dcterms:description
"[To analyse the gene expression profiles of the mouse genital tubercle (GT) during urethral tube development at embryonic (E) days E14, E15, E16 and E17, as the aetiology of hypospadias, one of the most common congenital anomalies, remains unknown.]. 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:16978288
;
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:NP469509.RAwlHDqb0LJ5QKtPjdMhzIyogwAubUOr1iIybQa5HRiHk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:41+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" .
}