@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP487831.RAb4FHHzDmTpTUyF187hycRPQbn_OVOhPBD2J3h-V-hTA
> .
@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:NP487831.RAb4FHHzDmTpTUyF187hycRPQbn_OVOhPBD2J3h-V-hTA130_head
{
this:
np:hasAssertion
dgn-np:NP487831.RAb4FHHzDmTpTUyF187hycRPQbn_OVOhPBD2J3h-V-hTA130_assertion
;
np:hasProvenance
dgn-np:NP487831.RAb4FHHzDmTpTUyF187hycRPQbn_OVOhPBD2J3h-V-hTA130_provenance
;
np:hasPublicationInfo
dgn-np:NP487831.RAb4FHHzDmTpTUyF187hycRPQbn_OVOhPBD2J3h-V-hTA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP487831.RAb4FHHzDmTpTUyF187hycRPQbn_OVOhPBD2J3h-V-hTA130_assertion
a
np:Assertion
.
dgn-np:NP487831.RAb4FHHzDmTpTUyF187hycRPQbn_OVOhPBD2J3h-V-hTA130_provenance
a
np:Provenance
.
dgn-np:NP487831.RAb4FHHzDmTpTUyF187hycRPQbn_OVOhPBD2J3h-V-hTA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP487831.RAb4FHHzDmTpTUyF187hycRPQbn_OVOhPBD2J3h-V-hTA130_assertion
{
miriam-gene:65057
a
ncit:C16612
.
lld:C0017606
a
ncit:C7057
.
dgn-gda:DGNdbea0eb0245cb832d026798dd1e5e426
sio:SIO_000628
miriam-gene:65057
,
lld:C0017606
;
a
sio:SIO_001121
.
}
dgn-np:NP487831.RAb4FHHzDmTpTUyF187hycRPQbn_OVOhPBD2J3h-V-hTA130_provenance
{
dgn-np:NP487831.RAb4FHHzDmTpTUyF187hycRPQbn_OVOhPBD2J3h-V-hTA130_assertion
dcterms:description
"[The lack of association between the PACG susceptibility loci with ACD or AL suggests that predilection to PACG may be mediated by factors other than shallow anterior chamber or short eyeball length.]. 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:23920366
;
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:NP487831.RAb4FHHzDmTpTUyF187hycRPQbn_OVOhPBD2J3h-V-hTA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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" .
}