@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP162755.RAHg6mCGWOSsU0Gb01Qm1VSNEoCt1S8NQ8cvmMfaUoC4A
> .
@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:NP162755.RAHg6mCGWOSsU0Gb01Qm1VSNEoCt1S8NQ8cvmMfaUoC4A130_head
{
this:
np:hasAssertion
dgn-np:NP162755.RAHg6mCGWOSsU0Gb01Qm1VSNEoCt1S8NQ8cvmMfaUoC4A130_assertion
;
np:hasProvenance
dgn-np:NP162755.RAHg6mCGWOSsU0Gb01Qm1VSNEoCt1S8NQ8cvmMfaUoC4A130_provenance
;
np:hasPublicationInfo
dgn-np:NP162755.RAHg6mCGWOSsU0Gb01Qm1VSNEoCt1S8NQ8cvmMfaUoC4A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP162755.RAHg6mCGWOSsU0Gb01Qm1VSNEoCt1S8NQ8cvmMfaUoC4A130_assertion
a
np:Assertion
.
dgn-np:NP162755.RAHg6mCGWOSsU0Gb01Qm1VSNEoCt1S8NQ8cvmMfaUoC4A130_provenance
a
np:Provenance
.
dgn-np:NP162755.RAHg6mCGWOSsU0Gb01Qm1VSNEoCt1S8NQ8cvmMfaUoC4A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP162755.RAHg6mCGWOSsU0Gb01Qm1VSNEoCt1S8NQ8cvmMfaUoC4A130_assertion
{
miriam-gene:6520
a
ncit:C16612
.
lld:C0023434
a
ncit:C7057
.
dgn-gda:DGN35ce6243b5e2a9be1c2826d18d48c7cd
sio:SIO_000628
miriam-gene:6520
,
lld:C0023434
;
a
sio:SIO_001121
.
}
dgn-np:NP162755.RAHg6mCGWOSsU0Gb01Qm1VSNEoCt1S8NQ8cvmMfaUoC4A130_provenance
{
dgn-np:NP162755.RAHg6mCGWOSsU0Gb01Qm1VSNEoCt1S8NQ8cvmMfaUoC4A130_assertion
dcterms:description
"[In order to further investigate the T393C SNP in CLL, we have genotyped 279 CLL cases and correlated the genotypes to clinical outcome and other known prognostic factors such as the immunoglobulin heavy chain variable (IGHV) gene mutation status and CD38 expression.]. 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:18006055
;
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:NP162755.RAHg6mCGWOSsU0Gb01Qm1VSNEoCt1S8NQ8cvmMfaUoC4A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:28+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" .
}