@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP497016.RAppPELZKizWnPWXbNt81o9jiQ96qbUDBcq7p16aavj44
> .
@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:NP497016.RAppPELZKizWnPWXbNt81o9jiQ96qbUDBcq7p16aavj44130_head
{
this:
np:hasAssertion
dgn-np:NP497016.RAppPELZKizWnPWXbNt81o9jiQ96qbUDBcq7p16aavj44130_assertion
;
np:hasProvenance
dgn-np:NP497016.RAppPELZKizWnPWXbNt81o9jiQ96qbUDBcq7p16aavj44130_provenance
;
np:hasPublicationInfo
dgn-np:NP497016.RAppPELZKizWnPWXbNt81o9jiQ96qbUDBcq7p16aavj44130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP497016.RAppPELZKizWnPWXbNt81o9jiQ96qbUDBcq7p16aavj44130_assertion
a
np:Assertion
.
dgn-np:NP497016.RAppPELZKizWnPWXbNt81o9jiQ96qbUDBcq7p16aavj44130_provenance
a
np:Provenance
.
dgn-np:NP497016.RAppPELZKizWnPWXbNt81o9jiQ96qbUDBcq7p16aavj44130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP497016.RAppPELZKizWnPWXbNt81o9jiQ96qbUDBcq7p16aavj44130_assertion
{
miriam-gene:154
a
ncit:C16612
.
lld:C1533041
a
ncit:C7057
.
dgn-gda:DGN62d3ed72c95f2122930bc3b6335ae8d5
sio:SIO_000628
miriam-gene:154
,
lld:C1533041
;
a
sio:SIO_001121
.
}
dgn-np:NP497016.RAppPELZKizWnPWXbNt81o9jiQ96qbUDBcq7p16aavj44130_provenance
{
dgn-np:NP497016.RAppPELZKizWnPWXbNt81o9jiQ96qbUDBcq7p16aavj44130_assertion
dcterms:description
"[These results suggest no evidence of an association between the Arg16Gly, Glu27Gln and Thr164Ile polymorphisms of the B2AR gene and risk of developing primary open angle glaucoma or primary congenital 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:13680034
;
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:NP497016.RAppPELZKizWnPWXbNt81o9jiQ96qbUDBcq7p16aavj44130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:56+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" .
}