@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0
> .
@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:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_head
{
this:
np:hasAssertion
dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_assertion
;
np:hasProvenance
dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_provenance
;
np:hasPublicationInfo
dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_assertion
a
np:Assertion
.
dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_provenance
a
np:Provenance
.
dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_assertion
{
miriam-gene:231
a
ncit:C16612
.
lld:C0848558
a
ncit:C7057
.
dgn-gda:DGN68e2ae615c6a70974e7f8b3bcb7ae912
sio:SIO_000628
miriam-gene:231
,
lld:C0848558
;
a
sio:SIO_001122
.
}
dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_provenance
{
dgn-np:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_assertion
dcterms:description
"[ This finding is in accordance with the assumption that functional polymorphisms may play an important role in complex disorders such as hypospadias when several genes as well as environmental factors contribute to the etiology.]. 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:16174723
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP48725.RA4mLSrwwuprm75SIItSLtgNwPxd3dG3VzowltjLHLGx0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}