@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP501091.RAsWBT4ofblVkYMJI5sTCd2Ns9nBndP0W8YfGhRZU6PvI
> .
@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:NP501091.RAsWBT4ofblVkYMJI5sTCd2Ns9nBndP0W8YfGhRZU6PvI130_head
{
this:
np:hasAssertion
dgn-np:NP501091.RAsWBT4ofblVkYMJI5sTCd2Ns9nBndP0W8YfGhRZU6PvI130_assertion
;
np:hasProvenance
dgn-np:NP501091.RAsWBT4ofblVkYMJI5sTCd2Ns9nBndP0W8YfGhRZU6PvI130_provenance
;
np:hasPublicationInfo
dgn-np:NP501091.RAsWBT4ofblVkYMJI5sTCd2Ns9nBndP0W8YfGhRZU6PvI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP501091.RAsWBT4ofblVkYMJI5sTCd2Ns9nBndP0W8YfGhRZU6PvI130_assertion
a
np:Assertion
.
dgn-np:NP501091.RAsWBT4ofblVkYMJI5sTCd2Ns9nBndP0W8YfGhRZU6PvI130_provenance
a
np:Provenance
.
dgn-np:NP501091.RAsWBT4ofblVkYMJI5sTCd2Ns9nBndP0W8YfGhRZU6PvI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP501091.RAsWBT4ofblVkYMJI5sTCd2Ns9nBndP0W8YfGhRZU6PvI130_assertion
{
miriam-gene:5309
a
ncit:C16612
.
lld:C0026010
a
ncit:C7057
.
dgn-gda:DGN91951c79ccb44cc9ac20a28111ae40cf
sio:SIO_000628
miriam-gene:5309
,
lld:C0026010
;
a
sio:SIO_001121
.
}
dgn-np:NP501091.RAsWBT4ofblVkYMJI5sTCd2Ns9nBndP0W8YfGhRZU6PvI130_provenance
{
dgn-np:NP501091.RAsWBT4ofblVkYMJI5sTCd2Ns9nBndP0W8YfGhRZU6PvI130_assertion
dcterms:description
"[Heterozygous missense mutations in PITX3 have been reported in patients with autosomal dominant congenital cataract and anterior segment (ocular) mesenchymal dysgenesis (ASMD) whereas homozygous missense mutations have been found in patients with microphthalmia and neurological impairment.]. 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:22223473
;
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:NP501091.RAsWBT4ofblVkYMJI5sTCd2Ns9nBndP0W8YfGhRZU6PvI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:58+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" .
}