@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP376506.RAFZTuxKzYqkTabZAy4_LAn4HHA8Wbn0azS68nFJQO3WI
> .
@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:NP376506.RAFZTuxKzYqkTabZAy4_LAn4HHA8Wbn0azS68nFJQO3WI130_head
{
this:
np:hasAssertion
dgn-np:NP376506.RAFZTuxKzYqkTabZAy4_LAn4HHA8Wbn0azS68nFJQO3WI130_assertion
;
np:hasProvenance
dgn-np:NP376506.RAFZTuxKzYqkTabZAy4_LAn4HHA8Wbn0azS68nFJQO3WI130_provenance
;
np:hasPublicationInfo
dgn-np:NP376506.RAFZTuxKzYqkTabZAy4_LAn4HHA8Wbn0azS68nFJQO3WI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP376506.RAFZTuxKzYqkTabZAy4_LAn4HHA8Wbn0azS68nFJQO3WI130_assertion
a
np:Assertion
.
dgn-np:NP376506.RAFZTuxKzYqkTabZAy4_LAn4HHA8Wbn0azS68nFJQO3WI130_provenance
a
np:Provenance
.
dgn-np:NP376506.RAFZTuxKzYqkTabZAy4_LAn4HHA8Wbn0azS68nFJQO3WI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP376506.RAFZTuxKzYqkTabZAy4_LAn4HHA8Wbn0azS68nFJQO3WI130_assertion
{
miriam-gene:959
a
ncit:C16612
.
lld:C0398686
a
ncit:C7057
.
dgn-gda:DGNec96f696932de6ec283f6d0a06414729
sio:SIO_000628
miriam-gene:959
,
lld:C0398686
;
a
sio:SIO_001121
.
}
dgn-np:NP376506.RAFZTuxKzYqkTabZAy4_LAn4HHA8Wbn0azS68nFJQO3WI130_provenance
{
dgn-np:NP376506.RAFZTuxKzYqkTabZAy4_LAn4HHA8Wbn0azS68nFJQO3WI130_assertion
dcterms:description
"[The X-linked hyper-IgM (XHIGM) syndrome is an uncommon primary immunodeficiency disease caused by mutations in the gene for CD40 ligand and characterized by normal or elevated serum IgM, reduced levels of IgG and IgA, and defective T-cell function.]. 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:14663287
;
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:NP376506.RAFZTuxKzYqkTabZAy4_LAn4HHA8Wbn0azS68nFJQO3WI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:40+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" .
}