@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP275521.RASTOeSZ_WhFNVMLdZ8we_t5ZoEaMg0-CF0uw6mSaHkH8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP275521.RASTOeSZ_WhFNVMLdZ8we_t5ZoEaMg0-CF0uw6mSaHkH8130_head
{
this:
np:hasAssertion
dgn-np:NP275521.RASTOeSZ_WhFNVMLdZ8we_t5ZoEaMg0-CF0uw6mSaHkH8130_assertion
;
np:hasProvenance
dgn-np:NP275521.RASTOeSZ_WhFNVMLdZ8we_t5ZoEaMg0-CF0uw6mSaHkH8130_provenance
;
np:hasPublicationInfo
dgn-np:NP275521.RASTOeSZ_WhFNVMLdZ8we_t5ZoEaMg0-CF0uw6mSaHkH8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP275521.RASTOeSZ_WhFNVMLdZ8we_t5ZoEaMg0-CF0uw6mSaHkH8130_assertion
a
np:Assertion
.
dgn-np:NP275521.RASTOeSZ_WhFNVMLdZ8we_t5ZoEaMg0-CF0uw6mSaHkH8130_provenance
a
np:Provenance
.
dgn-np:NP275521.RASTOeSZ_WhFNVMLdZ8we_t5ZoEaMg0-CF0uw6mSaHkH8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP275521.RASTOeSZ_WhFNVMLdZ8we_t5ZoEaMg0-CF0uw6mSaHkH8130_assertion
{
miriam-gene:718
a
ncit:C16612
.
lld:C0004364
a
ncit:C7057
.
dgn-gda:DGN59d4cfddc6d5ae9808708a1af53afe69
sio:SIO_000628
miriam-gene:718
,
lld:C0004364
;
a
sio:SIO_001121
.
}
dgn-np:NP275521.RASTOeSZ_WhFNVMLdZ8we_t5ZoEaMg0-CF0uw6mSaHkH8130_provenance
{
dgn-np:NP275521.RASTOeSZ_WhFNVMLdZ8we_t5ZoEaMg0-CF0uw6mSaHkH8130_assertion
dcterms:description
"[Classical pathway deficiencies and low numeric expression of erythrocyte C3b receptors (CR1) are typically associated with autoimmune disorders, while alternative pathway, terminal component, and leukocyte iC3b receptor (CR3) defects predispose to pyogenic bacterial disease.]. 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:2941192
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP275521.RASTOeSZ_WhFNVMLdZ8we_t5ZoEaMg0-CF0uw6mSaHkH8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:17+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}