@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI
> .
@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:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_head
{
this:
np:hasAssertion
dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_assertion
;
np:hasProvenance
dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_provenance
;
np:hasPublicationInfo
dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_assertion
a
np:Assertion
.
dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_provenance
a
np:Provenance
.
dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_assertion
{
miriam-gene:5308
a
ncit:C16612
.
lld:C3495489
a
ncit:C7057
.
dgn-gda:DGNeda8681fd784e854204c9703e89563be
sio:SIO_000628
miriam-gene:5308
,
lld:C3495489
;
a
sio:SIO_001121
.
}
dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_provenance
{
dgn-np:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_assertion
dcterms:description
"[Given the lack of any novel genes near either breakpoint, changes in potential regulatory elements may be the best model to explain the loss of PITX2 expression in these patients and hence the Rieger's syndrome phenotype.]. 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:14991915
;
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:NP350354.RA46drHpINnBopAgbBS-coRtWSft1AgAA1rddSNgqeNuI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:25+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" .
}