@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM
> .
@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:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_head
{
this:
np:hasAssertion
dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_assertion
;
np:hasProvenance
dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_provenance
;
np:hasPublicationInfo
dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_assertion
a
np:Assertion
.
dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_provenance
a
np:Provenance
.
dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_assertion
{
miriam-gene:4988
a
ncit:C16612
.
lld:C0027708
a
ncit:C7057
.
dgn-gda:DGNd589256f8e0f19ae20304eb22d151529
sio:SIO_000628
miriam-gene:4988
,
lld:C0027708
;
a
sio:SIO_001121
.
}
dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_provenance
{
dgn-np:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_assertion
dcterms:description
"[On the basis of our male patient 1 and on further six male cases of the literature, we also highlighted that larger 19q13.11 deletions including the Wilms tumor interacting protein (WTIP) gene, proximal to the MOR, results in hypospadias making this gene a possible candidate for this genital abnormality due to its well-known interaction with WT1.]. 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:22378287
;
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:NP237672.RAROclqHHBXrdJswwfItD0o1odPgzCcisnMIjkCl8m9wM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:13+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
<
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> , <
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
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}