@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w
> .
@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:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_head
{
this:
np:hasAssertion
dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_assertion
;
np:hasProvenance
dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_provenance
;
np:hasPublicationInfo
dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_assertion
a
np:Assertion
.
dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_provenance
a
np:Provenance
.
dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_assertion
{
miriam-gene:3075
a
ncit:C16612
.
lld:C0022658
a
ncit:C7057
.
dgn-gda:DGN74ddcb2b2f499aac51401bfc57f1c231
sio:SIO_000628
miriam-gene:3075
,
lld:C0022658
;
a
sio:SIO_001121
.
}
dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_provenance
{
dgn-np:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_assertion
dcterms:description
"[Mutations in the Factor H gene are associated with severe and diverse diseases including the rare renal disorders hemolytic uremic syndrome (HUS) and membranoproliferative glomerulonephritis (MPGN) also termed dense deposit disease (DDD), as well as the more frequent retinal disease age related macular degeneration (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: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:NP876128.RAHAQazpA6rtNLliMNOt1T_iiOgr_GfUJzxxkngpkXR1w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:55+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" .
}