@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP264481.RAuU7y5AccX_z-I4RaFwQfqTh4-S37LTfIYhnlEh8KMHs
> .
@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:NP264481.RAuU7y5AccX_z-I4RaFwQfqTh4-S37LTfIYhnlEh8KMHs130_head
{
this:
np:hasAssertion
dgn-np:NP264481.RAuU7y5AccX_z-I4RaFwQfqTh4-S37LTfIYhnlEh8KMHs130_assertion
;
np:hasProvenance
dgn-np:NP264481.RAuU7y5AccX_z-I4RaFwQfqTh4-S37LTfIYhnlEh8KMHs130_provenance
;
np:hasPublicationInfo
dgn-np:NP264481.RAuU7y5AccX_z-I4RaFwQfqTh4-S37LTfIYhnlEh8KMHs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP264481.RAuU7y5AccX_z-I4RaFwQfqTh4-S37LTfIYhnlEh8KMHs130_assertion
a
np:Assertion
.
dgn-np:NP264481.RAuU7y5AccX_z-I4RaFwQfqTh4-S37LTfIYhnlEh8KMHs130_provenance
a
np:Provenance
.
dgn-np:NP264481.RAuU7y5AccX_z-I4RaFwQfqTh4-S37LTfIYhnlEh8KMHs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP264481.RAuU7y5AccX_z-I4RaFwQfqTh4-S37LTfIYhnlEh8KMHs130_assertion
{
miriam-gene:2837
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGNdb009c5cdc6086f58ebbd8d1e17872ae
sio:SIO_000628
miriam-gene:2837
,
lld:C0242383
;
a
sio:SIO_001121
.
}
dgn-np:NP264481.RAuU7y5AccX_z-I4RaFwQfqTh4-S37LTfIYhnlEh8KMHs130_provenance
{
dgn-np:NP264481.RAuU7y5AccX_z-I4RaFwQfqTh4-S37LTfIYhnlEh8KMHs130_assertion
dcterms:description
"[The lack of functional effects of the 3'UTR indel, the amino acid substitution of rs10490924 (A69S), and strong LD between them suggest that A69S, not the indel, is the variant that confers risk of AMD.]. 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:20182747
;
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:NP264481.RAuU7y5AccX_z-I4RaFwQfqTh4-S37LTfIYhnlEh8KMHs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:27+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" .
}