@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP599347.RAosR3pSYBrLFm6U5Bs6DlZg_ak_ql0w38HYJhFgdxzxo
> .
@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:NP599347.RAosR3pSYBrLFm6U5Bs6DlZg_ak_ql0w38HYJhFgdxzxo130_head
{
this:
np:hasAssertion
dgn-np:NP599347.RAosR3pSYBrLFm6U5Bs6DlZg_ak_ql0w38HYJhFgdxzxo130_assertion
;
np:hasProvenance
dgn-np:NP599347.RAosR3pSYBrLFm6U5Bs6DlZg_ak_ql0w38HYJhFgdxzxo130_provenance
;
np:hasPublicationInfo
dgn-np:NP599347.RAosR3pSYBrLFm6U5Bs6DlZg_ak_ql0w38HYJhFgdxzxo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP599347.RAosR3pSYBrLFm6U5Bs6DlZg_ak_ql0w38HYJhFgdxzxo130_assertion
a
np:Assertion
.
dgn-np:NP599347.RAosR3pSYBrLFm6U5Bs6DlZg_ak_ql0w38HYJhFgdxzxo130_provenance
a
np:Provenance
.
dgn-np:NP599347.RAosR3pSYBrLFm6U5Bs6DlZg_ak_ql0w38HYJhFgdxzxo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP599347.RAosR3pSYBrLFm6U5Bs6DlZg_ak_ql0w38HYJhFgdxzxo130_assertion
{
miriam-gene:387715
a
ncit:C16612
.
lld:C1536085
a
ncit:C7057
.
dgn-gda:DGNc88b92aa577fb844905f16e019bdea0e
sio:SIO_000628
miriam-gene:387715
,
lld:C1536085
;
a
sio:SIO_001121
.
}
dgn-np:NP599347.RAosR3pSYBrLFm6U5Bs6DlZg_ak_ql0w38HYJhFgdxzxo130_provenance
{
dgn-np:NP599347.RAosR3pSYBrLFm6U5Bs6DlZg_ak_ql0w38HYJhFgdxzxo130_assertion
dcterms:description
"[Analyses of other measures of GA progression (progression to central GA from extrafoveal GA and development of bilateral GA in those initially with unilateral GA) showed no statistically significant association between progression and the LOC387715/ARMS2/HTRA1 genotype.]. 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:20381870
;
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:NP599347.RAosR3pSYBrLFm6U5Bs6DlZg_ak_ql0w38HYJhFgdxzxo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:00+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" .
}