@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP281679.RAKM7e7B324msQQmEXRSo_Sp7kBo6HC0ztRXeNm1CrhPQ
> .
@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:NP281679.RAKM7e7B324msQQmEXRSo_Sp7kBo6HC0ztRXeNm1CrhPQ130_head
{
this:
np:hasAssertion
dgn-np:NP281679.RAKM7e7B324msQQmEXRSo_Sp7kBo6HC0ztRXeNm1CrhPQ130_assertion
;
np:hasProvenance
dgn-np:NP281679.RAKM7e7B324msQQmEXRSo_Sp7kBo6HC0ztRXeNm1CrhPQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP281679.RAKM7e7B324msQQmEXRSo_Sp7kBo6HC0ztRXeNm1CrhPQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP281679.RAKM7e7B324msQQmEXRSo_Sp7kBo6HC0ztRXeNm1CrhPQ130_assertion
a
np:Assertion
.
dgn-np:NP281679.RAKM7e7B324msQQmEXRSo_Sp7kBo6HC0ztRXeNm1CrhPQ130_provenance
a
np:Provenance
.
dgn-np:NP281679.RAKM7e7B324msQQmEXRSo_Sp7kBo6HC0ztRXeNm1CrhPQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP281679.RAKM7e7B324msQQmEXRSo_Sp7kBo6HC0ztRXeNm1CrhPQ130_assertion
{
miriam-gene:4653
a
ncit:C16612
.
lld:C0020302
a
ncit:C7057
.
dgn-gda:DGN75dc34fc44cdc8d8e8e2480f9bb19541
sio:SIO_000628
miriam-gene:4653
,
lld:C0020302
;
a
sio:SIO_001121
.
}
dgn-np:NP281679.RAKM7e7B324msQQmEXRSo_Sp7kBo6HC0ztRXeNm1CrhPQ130_provenance
{
dgn-np:NP281679.RAKM7e7B324msQQmEXRSo_Sp7kBo6HC0ztRXeNm1CrhPQ130_assertion
dcterms:description
"[Thus, it is important to screen other glaucoma-associated loci and genes for involvement in congenital glaucoma in cases that are either negative or heterozygous for MYOC, CYP1B1, and FOXC1 mutations to have better insight into the disease pathogenesis.]. 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:23378721
;
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:NP281679.RAKM7e7B324msQQmEXRSo_Sp7kBo6HC0ztRXeNm1CrhPQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:39+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" .
}