@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP534541.RAd5-3IuaudreTSmQYJOroqFrH8WOhJJyfyaJzqJBGU2E
> .
@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:NP534541.RAd5-3IuaudreTSmQYJOroqFrH8WOhJJyfyaJzqJBGU2E130_head
{
this:
np:hasAssertion
dgn-np:NP534541.RAd5-3IuaudreTSmQYJOroqFrH8WOhJJyfyaJzqJBGU2E130_assertion
;
np:hasProvenance
dgn-np:NP534541.RAd5-3IuaudreTSmQYJOroqFrH8WOhJJyfyaJzqJBGU2E130_provenance
;
np:hasPublicationInfo
dgn-np:NP534541.RAd5-3IuaudreTSmQYJOroqFrH8WOhJJyfyaJzqJBGU2E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP534541.RAd5-3IuaudreTSmQYJOroqFrH8WOhJJyfyaJzqJBGU2E130_assertion
a
np:Assertion
.
dgn-np:NP534541.RAd5-3IuaudreTSmQYJOroqFrH8WOhJJyfyaJzqJBGU2E130_provenance
a
np:Provenance
.
dgn-np:NP534541.RAd5-3IuaudreTSmQYJOroqFrH8WOhJJyfyaJzqJBGU2E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP534541.RAd5-3IuaudreTSmQYJOroqFrH8WOhJJyfyaJzqJBGU2E130_assertion
{
miriam-gene:2728
a
ncit:C16612
.
lld:C1533041
a
ncit:C7057
.
dgn-gda:DGNb9fbc1c369559feea6b4e10eba70f85b
sio:SIO_000628
miriam-gene:2728
,
lld:C1533041
;
a
sio:SIO_001121
.
}
dgn-np:NP534541.RAd5-3IuaudreTSmQYJOroqFrH8WOhJJyfyaJzqJBGU2E130_provenance
{
dgn-np:NP534541.RAd5-3IuaudreTSmQYJOroqFrH8WOhJJyfyaJzqJBGU2E130_assertion
dcterms:description
"[The autosomal recessive form of primary congenital glaucoma (gene symbol GLC3) has been recently mapped to two different loci, GLC3A (at 2p21), and GLC3B (at 1p36), respectively, on families of Turkish and Saudi Arabian provenance.]. 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:9463798
;
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:NP534541.RAd5-3IuaudreTSmQYJOroqFrH8WOhJJyfyaJzqJBGU2E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:22+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" .
}