@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP392849.RAEFl1IDFg4m289Vmy4LUaJuSq7g8JyhQ3maASf5j7b2k
> .
@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:NP392849.RAEFl1IDFg4m289Vmy4LUaJuSq7g8JyhQ3maASf5j7b2k130_head
{
this:
np:hasAssertion
dgn-np:NP392849.RAEFl1IDFg4m289Vmy4LUaJuSq7g8JyhQ3maASf5j7b2k130_assertion
;
np:hasProvenance
dgn-np:NP392849.RAEFl1IDFg4m289Vmy4LUaJuSq7g8JyhQ3maASf5j7b2k130_provenance
;
np:hasPublicationInfo
dgn-np:NP392849.RAEFl1IDFg4m289Vmy4LUaJuSq7g8JyhQ3maASf5j7b2k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP392849.RAEFl1IDFg4m289Vmy4LUaJuSq7g8JyhQ3maASf5j7b2k130_assertion
a
np:Assertion
.
dgn-np:NP392849.RAEFl1IDFg4m289Vmy4LUaJuSq7g8JyhQ3maASf5j7b2k130_provenance
a
np:Provenance
.
dgn-np:NP392849.RAEFl1IDFg4m289Vmy4LUaJuSq7g8JyhQ3maASf5j7b2k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP392849.RAEFl1IDFg4m289Vmy4LUaJuSq7g8JyhQ3maASf5j7b2k130_assertion
{
miriam-gene:959
a
ncit:C16612
.
lld:C0029118
a
ncit:C7057
.
dgn-gda:DGNd91cebf7667571508d52479bee730959
sio:SIO_000628
miriam-gene:959
,
lld:C0029118
;
a
sio:SIO_001121
.
}
dgn-np:NP392849.RAEFl1IDFg4m289Vmy4LUaJuSq7g8JyhQ3maASf5j7b2k130_provenance
{
dgn-np:NP392849.RAEFl1IDFg4m289Vmy4LUaJuSq7g8JyhQ3maASf5j7b2k130_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:NP392849.RAEFl1IDFg4m289Vmy4LUaJuSq7g8JyhQ3maASf5j7b2k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:54+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" .
}