@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP313890.RA8fXWGOpzitXntZASmEC19QHfmoeSi8DmZeLPpFfxqXE
> .
@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:NP313890.RA8fXWGOpzitXntZASmEC19QHfmoeSi8DmZeLPpFfxqXE130_head
{
this:
np:hasAssertion
dgn-np:NP313890.RA8fXWGOpzitXntZASmEC19QHfmoeSi8DmZeLPpFfxqXE130_assertion
;
np:hasProvenance
dgn-np:NP313890.RA8fXWGOpzitXntZASmEC19QHfmoeSi8DmZeLPpFfxqXE130_provenance
;
np:hasPublicationInfo
dgn-np:NP313890.RA8fXWGOpzitXntZASmEC19QHfmoeSi8DmZeLPpFfxqXE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP313890.RA8fXWGOpzitXntZASmEC19QHfmoeSi8DmZeLPpFfxqXE130_assertion
a
np:Assertion
.
dgn-np:NP313890.RA8fXWGOpzitXntZASmEC19QHfmoeSi8DmZeLPpFfxqXE130_provenance
a
np:Provenance
.
dgn-np:NP313890.RA8fXWGOpzitXntZASmEC19QHfmoeSi8DmZeLPpFfxqXE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP313890.RA8fXWGOpzitXntZASmEC19QHfmoeSi8DmZeLPpFfxqXE130_assertion
{
miriam-gene:1524
a
ncit:C16612
.
lld:C0024437
a
ncit:C7057
.
dgn-gda:DGN339312b92abc3408eb96b3122f6fc652
sio:SIO_000628
miriam-gene:1524
,
lld:C0024437
;
a
sio:SIO_001121
.
}
dgn-np:NP313890.RA8fXWGOpzitXntZASmEC19QHfmoeSi8DmZeLPpFfxqXE130_provenance
{
dgn-np:NP313890.RA8fXWGOpzitXntZASmEC19QHfmoeSi8DmZeLPpFfxqXE130_assertion
dcterms:description
"[Peripheral blood from 85 AMD patients and 105 subjects without AMD (controls), as well as ocular tissue from 40 pathological sections with AMD and two normal eye sections, were screened for V249I and T280M, two single nucleotide polymorphisms (SNPs) in CX3CR1.]. 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:15208270
;
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:NP313890.RA8fXWGOpzitXntZASmEC19QHfmoeSi8DmZeLPpFfxqXE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:00+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" .
}