@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP902760.RAX_cyKrOAiI20OVKB-fE3yiwjyuQscUP0zjxLAVnTQO4
> .
@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:NP902760.RAX_cyKrOAiI20OVKB-fE3yiwjyuQscUP0zjxLAVnTQO4130_head
{
this:
np:hasAssertion
dgn-np:NP902760.RAX_cyKrOAiI20OVKB-fE3yiwjyuQscUP0zjxLAVnTQO4130_assertion
;
np:hasProvenance
dgn-np:NP902760.RAX_cyKrOAiI20OVKB-fE3yiwjyuQscUP0zjxLAVnTQO4130_provenance
;
np:hasPublicationInfo
dgn-np:NP902760.RAX_cyKrOAiI20OVKB-fE3yiwjyuQscUP0zjxLAVnTQO4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP902760.RAX_cyKrOAiI20OVKB-fE3yiwjyuQscUP0zjxLAVnTQO4130_assertion
a
np:Assertion
.
dgn-np:NP902760.RAX_cyKrOAiI20OVKB-fE3yiwjyuQscUP0zjxLAVnTQO4130_provenance
a
np:Provenance
.
dgn-np:NP902760.RAX_cyKrOAiI20OVKB-fE3yiwjyuQscUP0zjxLAVnTQO4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP902760.RAX_cyKrOAiI20OVKB-fE3yiwjyuQscUP0zjxLAVnTQO4130_assertion
{
miriam-gene:6774
a
ncit:C16612
.
lld:C0026946
a
ncit:C7057
.
dgn-gda:DGN7533747599ce02eab567d4d814d2337e
sio:SIO_000628
miriam-gene:6774
,
lld:C0026946
;
a
sio:SIO_001121
.
}
dgn-np:NP902760.RAX_cyKrOAiI20OVKB-fE3yiwjyuQscUP0zjxLAVnTQO4130_provenance
{
dgn-np:NP902760.RAX_cyKrOAiI20OVKB-fE3yiwjyuQscUP0zjxLAVnTQO4130_assertion
dcterms:description
"[By contrast, CMC is one of the few key infections in patients with autosomal dominant hyper IgE syndrome (mutations in STAT3), and in rare patients with autosomal recessive predisposition to mucocutaneous and invasive fungal infections (mutation in CARD9).]. 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:20674321
;
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:NP902760.RAX_cyKrOAiI20OVKB-fE3yiwjyuQscUP0zjxLAVnTQO4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:14+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" .
}