@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP567994.RAOida-SimxytU6I5q1I62vstRcEIM3MAtxX9pVfwZ-IU
> .
@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:NP567994.RAOida-SimxytU6I5q1I62vstRcEIM3MAtxX9pVfwZ-IU130_head
{
this:
np:hasAssertion
dgn-np:NP567994.RAOida-SimxytU6I5q1I62vstRcEIM3MAtxX9pVfwZ-IU130_assertion
;
np:hasProvenance
dgn-np:NP567994.RAOida-SimxytU6I5q1I62vstRcEIM3MAtxX9pVfwZ-IU130_provenance
;
np:hasPublicationInfo
dgn-np:NP567994.RAOida-SimxytU6I5q1I62vstRcEIM3MAtxX9pVfwZ-IU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP567994.RAOida-SimxytU6I5q1I62vstRcEIM3MAtxX9pVfwZ-IU130_assertion
a
np:Assertion
.
dgn-np:NP567994.RAOida-SimxytU6I5q1I62vstRcEIM3MAtxX9pVfwZ-IU130_provenance
a
np:Provenance
.
dgn-np:NP567994.RAOida-SimxytU6I5q1I62vstRcEIM3MAtxX9pVfwZ-IU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP567994.RAOida-SimxytU6I5q1I62vstRcEIM3MAtxX9pVfwZ-IU130_assertion
{
miriam-gene:3075
a
ncit:C16612
.
lld:C0035309
a
ncit:C7057
.
dgn-gda:DGN43a3b594c7d0ed283858cf775caf52c5
sio:SIO_000628
miriam-gene:3075
,
lld:C0035309
;
a
sio:SIO_001121
.
}
dgn-np:NP567994.RAOida-SimxytU6I5q1I62vstRcEIM3MAtxX9pVfwZ-IU130_provenance
{
dgn-np:NP567994.RAOida-SimxytU6I5q1I62vstRcEIM3MAtxX9pVfwZ-IU130_assertion
dcterms:description
"[Sequence variations or mutations of one single gene, coding for the host regulator Factor H, form the basis for multiple, different disorders such as human renal and retinal diseases as well as infections.]. 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:19388168
;
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:NP567994.RAOida-SimxytU6I5q1I62vstRcEIM3MAtxX9pVfwZ-IU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:42+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" .
}