@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP436124.RAYjOyNcCikz4D3dxGMA4GxFMyquhGWRaGk4bS_WcAEes
> .
@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:NP436124.RAYjOyNcCikz4D3dxGMA4GxFMyquhGWRaGk4bS_WcAEes130_head
{
this:
np:hasAssertion
dgn-np:NP436124.RAYjOyNcCikz4D3dxGMA4GxFMyquhGWRaGk4bS_WcAEes130_assertion
;
np:hasProvenance
dgn-np:NP436124.RAYjOyNcCikz4D3dxGMA4GxFMyquhGWRaGk4bS_WcAEes130_provenance
;
np:hasPublicationInfo
dgn-np:NP436124.RAYjOyNcCikz4D3dxGMA4GxFMyquhGWRaGk4bS_WcAEes130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP436124.RAYjOyNcCikz4D3dxGMA4GxFMyquhGWRaGk4bS_WcAEes130_assertion
a
np:Assertion
.
dgn-np:NP436124.RAYjOyNcCikz4D3dxGMA4GxFMyquhGWRaGk4bS_WcAEes130_provenance
a
np:Provenance
.
dgn-np:NP436124.RAYjOyNcCikz4D3dxGMA4GxFMyquhGWRaGk4bS_WcAEes130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP436124.RAYjOyNcCikz4D3dxGMA4GxFMyquhGWRaGk4bS_WcAEes130_assertion
{
miriam-gene:7535
a
ncit:C16612
.
lld:C0432408
a
ncit:C7057
.
dgn-gda:DGNc0cd889e9263bc67c482eceb7c3a1751
sio:SIO_000628
miriam-gene:7535
,
lld:C0432408
;
a
sio:SIO_001121
.
}
dgn-np:NP436124.RAYjOyNcCikz4D3dxGMA4GxFMyquhGWRaGk4bS_WcAEes130_provenance
{
dgn-np:NP436124.RAYjOyNcCikz4D3dxGMA4GxFMyquhGWRaGk4bS_WcAEes130_assertion
dcterms:description
"[In combination with the three cytogenetic markers associated with a poor prognosis, i.e., deletions 17p13, 11q22 and trisomy 12, expression of LPL and IGVH mutational status performed equally well with regard to their predictive value for survival, both being more predictive than ZAP70.]. 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:16434371
;
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:NP436124.RAYjOyNcCikz4D3dxGMA4GxFMyquhGWRaGk4bS_WcAEes130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:18+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" .
}