@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc
> .
@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:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_head
{
this:
np:hasAssertion
dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_assertion
;
np:hasProvenance
dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_provenance
;
np:hasPublicationInfo
dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_assertion
a
np:Assertion
.
dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_provenance
a
np:Provenance
.
dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C0272236
a
ncit:C7057
.
dgn-gda:DGN5d1ce07ff708ea25c20a26e7a1a1b1f6
sio:SIO_000628
miriam-gene:4397
,
lld:C0272236
;
a
sio:SIO_001121
.
}
dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_provenance
{
dgn-np:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_assertion
dcterms:description
"[In this review we present data on clinical diseases with characteristic IgM abnormalities, including primary and secondary hyper IgM syndromes, autoimmune hemolytic anemia, cryoglobulinemia, primary biliary cirrhosis and multiple sclerosis and place the data in the perspective of the normal maturation of the immune response, including somatic mutation and genetic rearrangement.]. 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:22178509
;
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:NP390347.RAvObAIiYZ5-g4hGVvgJjPkQcpL2ht-wZwoqEs8dembUc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:52+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" .
}