@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP328908.RARNJwUNhvsQ8mbAPHAEcnBCEbTL5710ejZOwYAnYgqB0
> .
@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:NP328908.RARNJwUNhvsQ8mbAPHAEcnBCEbTL5710ejZOwYAnYgqB0130_head
{
this:
np:hasAssertion
dgn-np:NP328908.RARNJwUNhvsQ8mbAPHAEcnBCEbTL5710ejZOwYAnYgqB0130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP328908.RARNJwUNhvsQ8mbAPHAEcnBCEbTL5710ejZOwYAnYgqB0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP328908.RARNJwUNhvsQ8mbAPHAEcnBCEbTL5710ejZOwYAnYgqB0130_assertion
a
np:Assertion
.
dgn-np:NP328908.RARNJwUNhvsQ8mbAPHAEcnBCEbTL5710ejZOwYAnYgqB0130_provenance
a
np:Provenance
.
dgn-np:NP328908.RARNJwUNhvsQ8mbAPHAEcnBCEbTL5710ejZOwYAnYgqB0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP328908.RARNJwUNhvsQ8mbAPHAEcnBCEbTL5710ejZOwYAnYgqB0130_assertion
{
miriam-gene:8440
a
ncit:C16612
.
lld:C0152136
a
ncit:C7057
.
dgn-gda:DGN1a8005c2be6d1ce3d5396b35ac8a8240
sio:SIO_000628
miriam-gene:8440
,
lld:C0152136
;
a
sio:SIO_001121
.
}
dgn-np:NP328908.RARNJwUNhvsQ8mbAPHAEcnBCEbTL5710ejZOwYAnYgqB0130_provenance
{
dgn-np:NP328908.RARNJwUNhvsQ8mbAPHAEcnBCEbTL5710ejZOwYAnYgqB0130_assertion
dcterms:description
"[The D2S176 marker had the strongest significant association and it is located 24 kb from the nearest gene NCK2, which now becomes an important new candidate gene for future studies of its association with normal tension glaucoma.]. 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:18723748
;
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 .
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dgn-np:NP328908.RARNJwUNhvsQ8mbAPHAEcnBCEbTL5710ejZOwYAnYgqB0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:14+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
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"v2.1.0" .
}