@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP662229.RA9rI6qLkrV-ChD74Fz_xHPncmzswlXBZ40p1LpRROvnQ
> .
@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:NP662229.RA9rI6qLkrV-ChD74Fz_xHPncmzswlXBZ40p1LpRROvnQ130_head
{
this:
np:hasAssertion
dgn-np:NP662229.RA9rI6qLkrV-ChD74Fz_xHPncmzswlXBZ40p1LpRROvnQ130_assertion
;
np:hasProvenance
dgn-np:NP662229.RA9rI6qLkrV-ChD74Fz_xHPncmzswlXBZ40p1LpRROvnQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP662229.RA9rI6qLkrV-ChD74Fz_xHPncmzswlXBZ40p1LpRROvnQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP662229.RA9rI6qLkrV-ChD74Fz_xHPncmzswlXBZ40p1LpRROvnQ130_assertion
a
np:Assertion
.
dgn-np:NP662229.RA9rI6qLkrV-ChD74Fz_xHPncmzswlXBZ40p1LpRROvnQ130_provenance
a
np:Provenance
.
dgn-np:NP662229.RA9rI6qLkrV-ChD74Fz_xHPncmzswlXBZ40p1LpRROvnQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP662229.RA9rI6qLkrV-ChD74Fz_xHPncmzswlXBZ40p1LpRROvnQ130_assertion
{
miriam-gene:7483
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNe7e5f71e558e554b782d6b5fedba0144
sio:SIO_000628
miriam-gene:7483
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP662229.RA9rI6qLkrV-ChD74Fz_xHPncmzswlXBZ40p1LpRROvnQ130_provenance
{
dgn-np:NP662229.RA9rI6qLkrV-ChD74Fz_xHPncmzswlXBZ40p1LpRROvnQ130_assertion
dcterms:description
"[Because these WNT gene clusters might be fragile sites in the human genome, implication of WNT3 or WNT3A in cancer as well as implication of WNT14 or WNT14B in connective tissue disease and congenital joint malformation should be elucidated in the future.]. 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:12011973
;
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:NP662229.RA9rI6qLkrV-ChD74Fz_xHPncmzswlXBZ40p1LpRROvnQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:40+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" .
}