@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP845617.RA1mTtjc88m6Px6mo_Wf5blM83gr3xsEvWkFzUvTGQO8o
> .
@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:NP845617.RA1mTtjc88m6Px6mo_Wf5blM83gr3xsEvWkFzUvTGQO8o130_head
{
this:
np:hasAssertion
dgn-np:NP845617.RA1mTtjc88m6Px6mo_Wf5blM83gr3xsEvWkFzUvTGQO8o130_assertion
;
np:hasProvenance
dgn-np:NP845617.RA1mTtjc88m6Px6mo_Wf5blM83gr3xsEvWkFzUvTGQO8o130_provenance
;
np:hasPublicationInfo
dgn-np:NP845617.RA1mTtjc88m6Px6mo_Wf5blM83gr3xsEvWkFzUvTGQO8o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP845617.RA1mTtjc88m6Px6mo_Wf5blM83gr3xsEvWkFzUvTGQO8o130_assertion
a
np:Assertion
.
dgn-np:NP845617.RA1mTtjc88m6Px6mo_Wf5blM83gr3xsEvWkFzUvTGQO8o130_provenance
a
np:Provenance
.
dgn-np:NP845617.RA1mTtjc88m6Px6mo_Wf5blM83gr3xsEvWkFzUvTGQO8o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP845617.RA1mTtjc88m6Px6mo_Wf5blM83gr3xsEvWkFzUvTGQO8o130_assertion
{
miriam-gene:10896
a
ncit:C16612
.
lld:C0017601
a
ncit:C7057
.
dgn-gda:DGN605cdaf63022e995dbafe674e511298b
sio:SIO_000628
miriam-gene:10896
,
lld:C0017601
;
a
sio:SIO_001121
.
}
dgn-np:NP845617.RA1mTtjc88m6Px6mo_Wf5blM83gr3xsEvWkFzUvTGQO8o130_provenance
{
dgn-np:NP845617.RA1mTtjc88m6Px6mo_Wf5blM83gr3xsEvWkFzUvTGQO8o130_assertion
dcterms:description
"[The entire TISR/oculomedin coding sequence, together with 138 bp of promoter sequence 5' to the start codon and 170 bp of the 3' untranslated region in 110 Chinese POAG patients and 108 unrelated control subjects without glaucoma, aged 50 years or above, were screened for alterations by DNA sequencing.]. 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:11129344
;
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:NP845617.RA1mTtjc88m6Px6mo_Wf5blM83gr3xsEvWkFzUvTGQO8o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:37+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" .
}