@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA
> .
@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:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_head
{
this:
np:hasAssertion
dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_assertion
;
np:hasProvenance
dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_provenance
;
np:hasPublicationInfo
dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_assertion
a
np:Assertion
.
dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_provenance
a
np:Provenance
.
dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_assertion
{
miriam-gene:9033
a
ncit:C16612
.
lld:C1136084
a
ncit:C7057
.
dgn-gda:DGN8188829508461ddd01af377e204c4488
sio:SIO_000628
miriam-gene:9033
,
lld:C1136084
;
a
sio:SIO_001121
.
}
dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_provenance
{
dgn-np:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_assertion
dcterms:description
"[To provide insights into the molecular characterization of plasma cell dyscrasias and to investigate the contribution of specific genetic lesions to the biological and clinical heterogeneity of MM, we analysed the gene expression profiles of plasma cells isolated from seven MGUS, 39 MM and six PCL patients by means of DNA microarrays.]. 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:15735737
;
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:NP817129.RAAcgk14z1LmN672dgKh6rSd6K3Fqng7Rug2uFnsywGaA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:20+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" .
}