@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP471322.RAKF0A17TcQuOTNPjHC7mw9m7vm_Uy0R-dO4a93YAsKds
> .
@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:NP471322.RAKF0A17TcQuOTNPjHC7mw9m7vm_Uy0R-dO4a93YAsKds130_head
{
this:
np:hasAssertion
dgn-np:NP471322.RAKF0A17TcQuOTNPjHC7mw9m7vm_Uy0R-dO4a93YAsKds130_assertion
;
np:hasProvenance
dgn-np:NP471322.RAKF0A17TcQuOTNPjHC7mw9m7vm_Uy0R-dO4a93YAsKds130_provenance
;
np:hasPublicationInfo
dgn-np:NP471322.RAKF0A17TcQuOTNPjHC7mw9m7vm_Uy0R-dO4a93YAsKds130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP471322.RAKF0A17TcQuOTNPjHC7mw9m7vm_Uy0R-dO4a93YAsKds130_assertion
a
np:Assertion
.
dgn-np:NP471322.RAKF0A17TcQuOTNPjHC7mw9m7vm_Uy0R-dO4a93YAsKds130_provenance
a
np:Provenance
.
dgn-np:NP471322.RAKF0A17TcQuOTNPjHC7mw9m7vm_Uy0R-dO4a93YAsKds130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP471322.RAKF0A17TcQuOTNPjHC7mw9m7vm_Uy0R-dO4a93YAsKds130_assertion
{
miriam-gene:100293534
a
ncit:C16612
.
lld:C0268731
a
ncit:C7057
.
dgn-gda:DGN42e180c86961503fc999bd671b64de65
sio:SIO_000628
miriam-gene:100293534
,
lld:C0268731
;
a
sio:SIO_001121
.
}
dgn-np:NP471322.RAKF0A17TcQuOTNPjHC7mw9m7vm_Uy0R-dO4a93YAsKds130_provenance
{
dgn-np:NP471322.RAKF0A17TcQuOTNPjHC7mw9m7vm_Uy0R-dO4a93YAsKds130_assertion
dcterms:description
"[These findings challenge the putative pathophysiological roles of C4A and C4B and underscore the need to perform functional assays, C4 allotyping and genotyping on patients with persistently low serum levels of a classical pathway complement component and glomerulopathy associated with immune deposits.]. 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:20580617
;
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:NP471322.RAKF0A17TcQuOTNPjHC7mw9m7vm_Uy0R-dO4a93YAsKds130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:42+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" .
}