@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP725162.RAmfl95nG2unJaAoGP-V3FySLQBAgPNq0l_-BsOYapRW4
> .
@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:NP725162.RAmfl95nG2unJaAoGP-V3FySLQBAgPNq0l_-BsOYapRW4130_head
{
this:
np:hasAssertion
dgn-np:NP725162.RAmfl95nG2unJaAoGP-V3FySLQBAgPNq0l_-BsOYapRW4130_assertion
;
np:hasProvenance
dgn-np:NP725162.RAmfl95nG2unJaAoGP-V3FySLQBAgPNq0l_-BsOYapRW4130_provenance
;
np:hasPublicationInfo
dgn-np:NP725162.RAmfl95nG2unJaAoGP-V3FySLQBAgPNq0l_-BsOYapRW4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP725162.RAmfl95nG2unJaAoGP-V3FySLQBAgPNq0l_-BsOYapRW4130_assertion
a
np:Assertion
.
dgn-np:NP725162.RAmfl95nG2unJaAoGP-V3FySLQBAgPNq0l_-BsOYapRW4130_provenance
a
np:Provenance
.
dgn-np:NP725162.RAmfl95nG2unJaAoGP-V3FySLQBAgPNq0l_-BsOYapRW4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP725162.RAmfl95nG2unJaAoGP-V3FySLQBAgPNq0l_-BsOYapRW4130_assertion
{
miriam-gene:7448
a
ncit:C16612
.
lld:C0242383
a
ncit:C7057
.
dgn-gda:DGN221b7c1715f7414c4166c78585c7e7cb
sio:SIO_000628
miriam-gene:7448
,
lld:C0242383
;
a
sio:SIO_001121
.
}
dgn-np:NP725162.RAmfl95nG2unJaAoGP-V3FySLQBAgPNq0l_-BsOYapRW4130_provenance
{
dgn-np:NP725162.RAmfl95nG2unJaAoGP-V3FySLQBAgPNq0l_-BsOYapRW4130_assertion
dcterms:description
"[The prevalence of homozygous carriers in regard to CFH Y402H polymorphism, which is suspicious for AMD, might be associated with increased secretion of vitronectin in response to dysregulation of the complement cascade.]. 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:17704937
;
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:NP725162.RAmfl95nG2unJaAoGP-V3FySLQBAgPNq0l_-BsOYapRW4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:20+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" .
}