@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP477298.RAX08KfQ6_ymIldIsaa0UHWUPS9rljlOeUXUJJgfpmhfw
> .
@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:NP477298.RAX08KfQ6_ymIldIsaa0UHWUPS9rljlOeUXUJJgfpmhfw130_head
{
this:
np:hasAssertion
dgn-np:NP477298.RAX08KfQ6_ymIldIsaa0UHWUPS9rljlOeUXUJJgfpmhfw130_assertion
;
np:hasProvenance
dgn-np:NP477298.RAX08KfQ6_ymIldIsaa0UHWUPS9rljlOeUXUJJgfpmhfw130_provenance
;
np:hasPublicationInfo
dgn-np:NP477298.RAX08KfQ6_ymIldIsaa0UHWUPS9rljlOeUXUJJgfpmhfw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP477298.RAX08KfQ6_ymIldIsaa0UHWUPS9rljlOeUXUJJgfpmhfw130_assertion
a
np:Assertion
.
dgn-np:NP477298.RAX08KfQ6_ymIldIsaa0UHWUPS9rljlOeUXUJJgfpmhfw130_provenance
a
np:Provenance
.
dgn-np:NP477298.RAX08KfQ6_ymIldIsaa0UHWUPS9rljlOeUXUJJgfpmhfw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP477298.RAX08KfQ6_ymIldIsaa0UHWUPS9rljlOeUXUJJgfpmhfw130_assertion
{
miriam-gene:3664
a
ncit:C16612
.
lld:C1837217
a
ncit:C7057
.
dgn-gda:DGNcfa0045a449d878b8b564b1b3bdda9c2
sio:SIO_000628
miriam-gene:3664
,
lld:C1837217
;
a
sio:SIO_001121
.
}
dgn-np:NP477298.RAX08KfQ6_ymIldIsaa0UHWUPS9rljlOeUXUJJgfpmhfw130_provenance
{
dgn-np:NP477298.RAX08KfQ6_ymIldIsaa0UHWUPS9rljlOeUXUJJgfpmhfw130_assertion
dcterms:description
"[It has been suggested to be an important contributor to orofacial development since mutations of the IRF6 gene has been found in Van der Woude (VWS) and popliteal pterygium syndromes (PPS), two disorders that can present with isolated cleft lip and palate.]. 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:23510002
;
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:NP477298.RAX08KfQ6_ymIldIsaa0UHWUPS9rljlOeUXUJJgfpmhfw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:46+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" .
}