@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP923646.RAwsc04A3sFZkbssMns67yKtjCFU1mUFiAptDTmEA1uvY
> .
@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:NP923646.RAwsc04A3sFZkbssMns67yKtjCFU1mUFiAptDTmEA1uvY130_head
{
this:
np:hasAssertion
dgn-np:NP923646.RAwsc04A3sFZkbssMns67yKtjCFU1mUFiAptDTmEA1uvY130_assertion
;
np:hasProvenance
dgn-np:NP923646.RAwsc04A3sFZkbssMns67yKtjCFU1mUFiAptDTmEA1uvY130_provenance
;
np:hasPublicationInfo
dgn-np:NP923646.RAwsc04A3sFZkbssMns67yKtjCFU1mUFiAptDTmEA1uvY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP923646.RAwsc04A3sFZkbssMns67yKtjCFU1mUFiAptDTmEA1uvY130_assertion
a
np:Assertion
.
dgn-np:NP923646.RAwsc04A3sFZkbssMns67yKtjCFU1mUFiAptDTmEA1uvY130_provenance
a
np:Provenance
.
dgn-np:NP923646.RAwsc04A3sFZkbssMns67yKtjCFU1mUFiAptDTmEA1uvY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP923646.RAwsc04A3sFZkbssMns67yKtjCFU1mUFiAptDTmEA1uvY130_assertion
{
miriam-gene:8140
a
ncit:C16612
.
lld:C1691215
a
ncit:C7057
.
dgn-gda:DGNebe6667108a252762f1f3b3b2d9d8811
sio:SIO_000628
miriam-gene:8140
,
lld:C1691215
;
a
sio:SIO_001121
.
}
dgn-np:NP923646.RAwsc04A3sFZkbssMns67yKtjCFU1mUFiAptDTmEA1uvY130_provenance
{
dgn-np:NP923646.RAwsc04A3sFZkbssMns67yKtjCFU1mUFiAptDTmEA1uvY130_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:NP923646.RAwsc04A3sFZkbssMns67yKtjCFU1mUFiAptDTmEA1uvY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:26+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" .
}