@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP194324.RABt-8tNRxuYnx6PGrwdIJOJWCjVQjclthGiamOCISjwQ
> .
@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:NP194324.RABt-8tNRxuYnx6PGrwdIJOJWCjVQjclthGiamOCISjwQ130_head
{
this:
np:hasAssertion
dgn-np:NP194324.RABt-8tNRxuYnx6PGrwdIJOJWCjVQjclthGiamOCISjwQ130_assertion
;
np:hasProvenance
dgn-np:NP194324.RABt-8tNRxuYnx6PGrwdIJOJWCjVQjclthGiamOCISjwQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP194324.RABt-8tNRxuYnx6PGrwdIJOJWCjVQjclthGiamOCISjwQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP194324.RABt-8tNRxuYnx6PGrwdIJOJWCjVQjclthGiamOCISjwQ130_assertion
a
np:Assertion
.
dgn-np:NP194324.RABt-8tNRxuYnx6PGrwdIJOJWCjVQjclthGiamOCISjwQ130_provenance
a
np:Provenance
.
dgn-np:NP194324.RABt-8tNRxuYnx6PGrwdIJOJWCjVQjclthGiamOCISjwQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP194324.RABt-8tNRxuYnx6PGrwdIJOJWCjVQjclthGiamOCISjwQ130_assertion
{
miriam-gene:3075
a
ncit:C16612
.
lld:C0017665
a
ncit:C7057
.
dgn-gda:DGNeee377951e92c099890c102de38b3e53
sio:SIO_000628
miriam-gene:3075
,
lld:C0017665
;
a
sio:SIO_001121
.
}
dgn-np:NP194324.RABt-8tNRxuYnx6PGrwdIJOJWCjVQjclthGiamOCISjwQ130_provenance
{
dgn-np:NP194324.RABt-8tNRxuYnx6PGrwdIJOJWCjVQjclthGiamOCISjwQ130_assertion
dcterms:description
"[In order to elucidate the regulatory mechanism of complement activation, we demonstrated glomerular deposition and urinary excretion of complement factor H, which controls the alternative pathway and the amplification loop at the C3 step, in patients with idiopathic MN.]. 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:15331938
;
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:NP194324.RABt-8tNRxuYnx6PGrwdIJOJWCjVQjclthGiamOCISjwQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:47+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" .
}