@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP249333.RA8xnOK8f3Hk6Q13rOboaAatJNQv9_yaO8MMJIODXZTGo
> .
@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:NP249333.RA8xnOK8f3Hk6Q13rOboaAatJNQv9_yaO8MMJIODXZTGo130_head
{
this:
np:hasAssertion
dgn-np:NP249333.RA8xnOK8f3Hk6Q13rOboaAatJNQv9_yaO8MMJIODXZTGo130_assertion
;
np:hasProvenance
dgn-np:NP249333.RA8xnOK8f3Hk6Q13rOboaAatJNQv9_yaO8MMJIODXZTGo130_provenance
;
np:hasPublicationInfo
dgn-np:NP249333.RA8xnOK8f3Hk6Q13rOboaAatJNQv9_yaO8MMJIODXZTGo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP249333.RA8xnOK8f3Hk6Q13rOboaAatJNQv9_yaO8MMJIODXZTGo130_assertion
a
np:Assertion
.
dgn-np:NP249333.RA8xnOK8f3Hk6Q13rOboaAatJNQv9_yaO8MMJIODXZTGo130_provenance
a
np:Provenance
.
dgn-np:NP249333.RA8xnOK8f3Hk6Q13rOboaAatJNQv9_yaO8MMJIODXZTGo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP249333.RA8xnOK8f3Hk6Q13rOboaAatJNQv9_yaO8MMJIODXZTGo130_assertion
{
miriam-gene:4016
a
ncit:C16612
.
lld:C0339573
a
ncit:C7057
.
dgn-gda:DGN8a8375f68b1a5c888891a69e9f83ac6a
sio:SIO_000628
miriam-gene:4016
,
lld:C0339573
;
a
sio:SIO_001121
.
}
dgn-np:NP249333.RA8xnOK8f3Hk6Q13rOboaAatJNQv9_yaO8MMJIODXZTGo130_provenance
{
dgn-np:NP249333.RA8xnOK8f3Hk6Q13rOboaAatJNQv9_yaO8MMJIODXZTGo130_assertion
dcterms:description
"[Two LOXL1 single nucleotide polymorphisms (SNPs), rs1048661 (R141L) and rs3825942 (G153D), were analyzed in 300 Turkish patients (100 patients with XFS, 100 patients with XFG, 100 patients with POAG) and 100 control subjects.]. 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:23378724
;
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:NP249333.RA8xnOK8f3Hk6Q13rOboaAatJNQv9_yaO8MMJIODXZTGo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:19+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" .
}