@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE
> .
@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:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_head
{
this:
np:hasAssertion
dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_assertion
;
np:hasProvenance
dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_provenance
;
np:hasPublicationInfo
dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_assertion
a
np:Assertion
.
dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_provenance
a
np:Provenance
.
dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_assertion
{
miriam-gene:23541
a
ncit:C16612
.
lld:C0026764
a
ncit:C7057
.
dgn-gda:DGNc1e8731c5b51fce5313b91503870a9ba
sio:SIO_000628
miriam-gene:23541
,
lld:C0026764
;
a
sio:SIO_001121
.
}
dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_provenance
{
dgn-np:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_assertion
dcterms:description
"[The higher risk that is associated with CA compared with SPF justifies routine cytogenetic studies in all patients with MM at diagnosis and whenever additional treatment decisions are considered, such as in planning HDT either for initial response consolidation, at the time of primary unresponsiveness to induction therapy, or at relapse.]. 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:12877670
;
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:NP246338.RAgQpFygRmSaT6DOyEvH2EKxk5zBM1poHv5aEP98mddFE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:18+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" .
}