@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU
> .
@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:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_head
{
this:
np:hasAssertion
dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_assertion
;
np:hasProvenance
dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_provenance
;
np:hasPublicationInfo
dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_assertion
a
np:Assertion
.
dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_provenance
a
np:Provenance
.
dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_assertion
{
miriam-gene:57379
a
ncit:C16612
.
lld:C0002871
a
ncit:C7057
.
dgn-gda:DGNcc04f904add38e4a6e145779c271150b
sio:SIO_000628
miriam-gene:57379
,
lld:C0002871
;
a
sio:SIO_001121
.
}
dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_provenance
{
dgn-np:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_assertion
dcterms:description
"[In the group of patients with hyper IgM syndrome, the patients with mutations in AID were older at the age of diagnosis, were more likely to have positive isohemagglutinins, and were less likely to have anemia, neutropenia, or thrombocytopenia.]. 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:11112359
;
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:NP921206.RAdbWpwVfZg7WRog8oAceMjz5D9XwAvhZ0IrrfvDziiUU130_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" .
}