@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP744506.RA70CB9SEWmKM20QN2ILY9mP4DYi8lq6PjPNG-2eHdBfk
> .
@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:NP744506.RA70CB9SEWmKM20QN2ILY9mP4DYi8lq6PjPNG-2eHdBfk130_head
{
this:
np:hasAssertion
dgn-np:NP744506.RA70CB9SEWmKM20QN2ILY9mP4DYi8lq6PjPNG-2eHdBfk130_assertion
;
np:hasProvenance
dgn-np:NP744506.RA70CB9SEWmKM20QN2ILY9mP4DYi8lq6PjPNG-2eHdBfk130_provenance
;
np:hasPublicationInfo
dgn-np:NP744506.RA70CB9SEWmKM20QN2ILY9mP4DYi8lq6PjPNG-2eHdBfk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP744506.RA70CB9SEWmKM20QN2ILY9mP4DYi8lq6PjPNG-2eHdBfk130_assertion
a
np:Assertion
.
dgn-np:NP744506.RA70CB9SEWmKM20QN2ILY9mP4DYi8lq6PjPNG-2eHdBfk130_provenance
a
np:Provenance
.
dgn-np:NP744506.RA70CB9SEWmKM20QN2ILY9mP4DYi8lq6PjPNG-2eHdBfk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP744506.RA70CB9SEWmKM20QN2ILY9mP4DYi8lq6PjPNG-2eHdBfk130_assertion
{
miriam-gene:981
a
ncit:C16612
.
lld:C0026764
a
ncit:C7057
.
dgn-gda:DGN2cd9c4f0ac634d9a630992ca170530aa
sio:SIO_000628
miriam-gene:981
,
lld:C0026764
;
a
sio:SIO_001121
.
}
dgn-np:NP744506.RA70CB9SEWmKM20QN2ILY9mP4DYi8lq6PjPNG-2eHdBfk130_provenance
{
dgn-np:NP744506.RA70CB9SEWmKM20QN2ILY9mP4DYi8lq6PjPNG-2eHdBfk130_assertion
dcterms:description
"[We have genetically characterized a large Swedish family in which the concurrence of CDA III and myeloma or benign monoclonal gammopathy is significantly higher than expected and have found that the causative genetic defect for CDA III maps to an 11 cM interval within 15q21-q25.]. 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:7711721
;
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:NP744506.RA70CB9SEWmKM20QN2ILY9mP4DYi8lq6PjPNG-2eHdBfk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:31+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" .
}