@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw
> .
@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:NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_head
{
this:
np:hasAssertion
dgn-np:NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_assertion
;
np:hasProvenance
dgn-np:NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_provenance
;
np:hasPublicationInfo
dgn-np:NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_assertion
a
np:Assertion
.
dgn-np:NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_provenance
a
np:Provenance
.
dgn-np:NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_assertion
{
miriam-gene:1604
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGNda2f7f0f14ca1a63d5f34ba48df35792
sio:SIO_000628
miriam-gene:1604
,
lld:C0242383
;
a
sio:SIO_001121
.
}
dgn-np:NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_provenance
{
dgn-np:NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_assertion
dcterms:description
"[In a case-control sample that has shown the well established associations between AMD and variants in CFH, CFB and C3 there was absence of association with SNPs in CFP, CD46, CD55 and CD59.]. 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:22024702
;
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:NP395791.RAeWIJV1IXzfwLwBRllb09WfRdx4L4YCCjj1ZTjKHCXUw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:55+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" .
}