@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47891.RADPikocF6k5rpOG4paCPjxx8H_3mf4MXXTOU1h38os8w
> .
@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:NP47891.RADPikocF6k5rpOG4paCPjxx8H_3mf4MXXTOU1h38os8w130_head
{
this:
np:hasAssertion
dgn-np:NP47891.RADPikocF6k5rpOG4paCPjxx8H_3mf4MXXTOU1h38os8w130_assertion
;
np:hasProvenance
dgn-np:NP47891.RADPikocF6k5rpOG4paCPjxx8H_3mf4MXXTOU1h38os8w130_provenance
;
np:hasPublicationInfo
dgn-np:NP47891.RADPikocF6k5rpOG4paCPjxx8H_3mf4MXXTOU1h38os8w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47891.RADPikocF6k5rpOG4paCPjxx8H_3mf4MXXTOU1h38os8w130_assertion
a
np:Assertion
.
dgn-np:NP47891.RADPikocF6k5rpOG4paCPjxx8H_3mf4MXXTOU1h38os8w130_provenance
a
np:Provenance
.
dgn-np:NP47891.RADPikocF6k5rpOG4paCPjxx8H_3mf4MXXTOU1h38os8w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47891.RADPikocF6k5rpOG4paCPjxx8H_3mf4MXXTOU1h38os8w130_assertion
{
miriam-gene:581
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGNcde213c305b2eab2c7ca4c880e5c009b
sio:SIO_000628
miriam-gene:581
,
lld:C0023418
;
a
sio:SIO_001122
.
}
dgn-np:NP47891.RADPikocF6k5rpOG4paCPjxx8H_3mf4MXXTOU1h38os8w130_provenance
{
dgn-np:NP47891.RADPikocF6k5rpOG4paCPjxx8H_3mf4MXXTOU1h38os8w130_assertion
dcterms:description
"[ The presence of this single nucleotide polymorphism in CLL critically influences the response to treatment and overall survival. Given the relatively high prevalence of this polymorphism in the normal population, further prospective studies in CLL and other human malignancies are indicated.]. 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:15735127
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP47891.RADPikocF6k5rpOG4paCPjxx8H_3mf4MXXTOU1h38os8w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}