@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP279702.RAxfh6ArqNugzJuT20d00HoNDrh18zH0Zhb9XJl_9ouno
> .
@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:NP279702.RAxfh6ArqNugzJuT20d00HoNDrh18zH0Zhb9XJl_9ouno130_head
{
this:
np:hasAssertion
dgn-np:NP279702.RAxfh6ArqNugzJuT20d00HoNDrh18zH0Zhb9XJl_9ouno130_assertion
;
np:hasProvenance
dgn-np:NP279702.RAxfh6ArqNugzJuT20d00HoNDrh18zH0Zhb9XJl_9ouno130_provenance
;
np:hasPublicationInfo
dgn-np:NP279702.RAxfh6ArqNugzJuT20d00HoNDrh18zH0Zhb9XJl_9ouno130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP279702.RAxfh6ArqNugzJuT20d00HoNDrh18zH0Zhb9XJl_9ouno130_assertion
a
np:Assertion
.
dgn-np:NP279702.RAxfh6ArqNugzJuT20d00HoNDrh18zH0Zhb9XJl_9ouno130_provenance
a
np:Provenance
.
dgn-np:NP279702.RAxfh6ArqNugzJuT20d00HoNDrh18zH0Zhb9XJl_9ouno130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP279702.RAxfh6ArqNugzJuT20d00HoNDrh18zH0Zhb9XJl_9ouno130_assertion
{
miriam-gene:907
a
ncit:C16612
.
lld:C0595921
a
ncit:C7057
.
dgn-gda:DGN0e505c6c3771f0c3b4c425b57cd24d28
sio:SIO_000628
miriam-gene:907
,
lld:C0595921
;
a
sio:SIO_001121
.
}
dgn-np:NP279702.RAxfh6ArqNugzJuT20d00HoNDrh18zH0Zhb9XJl_9ouno130_provenance
{
dgn-np:NP279702.RAxfh6ArqNugzJuT20d00HoNDrh18zH0Zhb9XJl_9ouno130_assertion
dcterms:description
"[The CCT measurements should be considered to ensure proper interpretation of IOP measurements in the diagnosis and management of disorders in which the CCT or IOP readings are outside normal limits.]. 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:9787354
;
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:NP279702.RAxfh6ArqNugzJuT20d00HoNDrh18zH0Zhb9XJl_9ouno130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:38+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" .
}