@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP623909.RAyMTSmOIFreUYXh5O5IFzrk-_G9C7o81gnH9Gyp-zndg
> .
@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:NP623909.RAyMTSmOIFreUYXh5O5IFzrk-_G9C7o81gnH9Gyp-zndg130_head
{
this:
np:hasAssertion
dgn-np:NP623909.RAyMTSmOIFreUYXh5O5IFzrk-_G9C7o81gnH9Gyp-zndg130_assertion
;
np:hasProvenance
dgn-np:NP623909.RAyMTSmOIFreUYXh5O5IFzrk-_G9C7o81gnH9Gyp-zndg130_provenance
;
np:hasPublicationInfo
dgn-np:NP623909.RAyMTSmOIFreUYXh5O5IFzrk-_G9C7o81gnH9Gyp-zndg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP623909.RAyMTSmOIFreUYXh5O5IFzrk-_G9C7o81gnH9Gyp-zndg130_assertion
a
np:Assertion
.
dgn-np:NP623909.RAyMTSmOIFreUYXh5O5IFzrk-_G9C7o81gnH9Gyp-zndg130_provenance
a
np:Provenance
.
dgn-np:NP623909.RAyMTSmOIFreUYXh5O5IFzrk-_G9C7o81gnH9Gyp-zndg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP623909.RAyMTSmOIFreUYXh5O5IFzrk-_G9C7o81gnH9Gyp-zndg130_assertion
{
miriam-gene:3664
a
ncit:C16612
.
lld:C0008924
a
ncit:C7057
.
dgn-gda:DGNa339d5da4ef14c2f805eed38e25614bf
sio:SIO_000628
miriam-gene:3664
,
lld:C0008924
;
a
sio:SIO_001121
.
}
dgn-np:NP623909.RAyMTSmOIFreUYXh5O5IFzrk-_G9C7o81gnH9Gyp-zndg130_provenance
{
dgn-np:NP623909.RAyMTSmOIFreUYXh5O5IFzrk-_G9C7o81gnH9Gyp-zndg130_assertion
dcterms:description
"[Variation at IRF6 was responsible for 12 percent of the genetic contribution to cleft lip or palate and tripled the risk of recurrence in families that had already had one affected child.]. 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:15317890
;
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:NP623909.RAyMTSmOIFreUYXh5O5IFzrk-_G9C7o81gnH9Gyp-zndg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:16+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" .
}