@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP418473.RAEodjr14ZWvaZef8qwEpMf7-0UbPx0VoWItlZf0TDL2U
> .
@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:NP418473.RAEodjr14ZWvaZef8qwEpMf7-0UbPx0VoWItlZf0TDL2U130_head
{
this:
np:hasAssertion
dgn-np:NP418473.RAEodjr14ZWvaZef8qwEpMf7-0UbPx0VoWItlZf0TDL2U130_assertion
;
np:hasProvenance
dgn-np:NP418473.RAEodjr14ZWvaZef8qwEpMf7-0UbPx0VoWItlZf0TDL2U130_provenance
;
np:hasPublicationInfo
dgn-np:NP418473.RAEodjr14ZWvaZef8qwEpMf7-0UbPx0VoWItlZf0TDL2U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP418473.RAEodjr14ZWvaZef8qwEpMf7-0UbPx0VoWItlZf0TDL2U130_assertion
a
np:Assertion
.
dgn-np:NP418473.RAEodjr14ZWvaZef8qwEpMf7-0UbPx0VoWItlZf0TDL2U130_provenance
a
np:Provenance
.
dgn-np:NP418473.RAEodjr14ZWvaZef8qwEpMf7-0UbPx0VoWItlZf0TDL2U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP418473.RAEodjr14ZWvaZef8qwEpMf7-0UbPx0VoWItlZf0TDL2U130_assertion
{
miriam-gene:959
a
ncit:C16612
.
lld:C0272236
a
ncit:C7057
.
dgn-gda:DGNb88ec32de0acb1dd2090b5cbc1b47c30
sio:SIO_000628
miriam-gene:959
,
lld:C0272236
;
a
sio:SIO_001121
.
}
dgn-np:NP418473.RAEodjr14ZWvaZef8qwEpMf7-0UbPx0VoWItlZf0TDL2U130_provenance
{
dgn-np:NP418473.RAEodjr14ZWvaZef8qwEpMf7-0UbPx0VoWItlZf0TDL2U130_assertion
dcterms:description
"[Hyper-IgM syndrome type 1 (HIGM1) is a primary immunodeficiency characterized by recurrent bacterial and opportunistic infections, associated with normal or high serum level of IgM and decreased serum levels of IgG, IgA and IgE due to the defect of class switch recombination.]. 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:16311023
;
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:NP418473.RAEodjr14ZWvaZef8qwEpMf7-0UbPx0VoWItlZf0TDL2U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:08+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" .
}