@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP921243.RAsiw3KQrLhSXGAaLhM-SGgASk1pqjyjYWjVAMwFlesOY
> .
@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:NP921243.RAsiw3KQrLhSXGAaLhM-SGgASk1pqjyjYWjVAMwFlesOY130_head
{
this:
np:hasAssertion
dgn-np:NP921243.RAsiw3KQrLhSXGAaLhM-SGgASk1pqjyjYWjVAMwFlesOY130_assertion
;
np:hasProvenance
dgn-np:NP921243.RAsiw3KQrLhSXGAaLhM-SGgASk1pqjyjYWjVAMwFlesOY130_provenance
;
np:hasPublicationInfo
dgn-np:NP921243.RAsiw3KQrLhSXGAaLhM-SGgASk1pqjyjYWjVAMwFlesOY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP921243.RAsiw3KQrLhSXGAaLhM-SGgASk1pqjyjYWjVAMwFlesOY130_assertion
a
np:Assertion
.
dgn-np:NP921243.RAsiw3KQrLhSXGAaLhM-SGgASk1pqjyjYWjVAMwFlesOY130_provenance
a
np:Provenance
.
dgn-np:NP921243.RAsiw3KQrLhSXGAaLhM-SGgASk1pqjyjYWjVAMwFlesOY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP921243.RAsiw3KQrLhSXGAaLhM-SGgASk1pqjyjYWjVAMwFlesOY130_assertion
{
miriam-gene:4153
a
ncit:C16612
.
lld:C0151317
a
ncit:C7057
.
dgn-gda:DGNc9254664f8526d19a45cfa60c63c3cd9
sio:SIO_000628
miriam-gene:4153
,
lld:C0151317
;
a
sio:SIO_001121
.
}
dgn-np:NP921243.RAsiw3KQrLhSXGAaLhM-SGgASk1pqjyjYWjVAMwFlesOY130_provenance
{
dgn-np:NP921243.RAsiw3KQrLhSXGAaLhM-SGgASk1pqjyjYWjVAMwFlesOY130_assertion
dcterms:description
"[Our data provides new information on the genetic instability of the C4 gene region, and on the association of homozygous C4B deficiency and variant MBL genotype with increased susceptibility to recurrent and chronic 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:12626442
;
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:NP921243.RAsiw3KQrLhSXGAaLhM-SGgASk1pqjyjYWjVAMwFlesOY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:25+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" .
}