@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ
> .
@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:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_head
{
this:
np:hasAssertion
dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_assertion
;
np:hasProvenance
dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_assertion
a
np:Assertion
.
dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_provenance
a
np:Provenance
.
dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_assertion
{
miriam-gene:4255
a
ncit:C16612
.
lld:C2939419
a
ncit:C7057
.
dgn-gda:DGN5c16f7d7f4ecb14eb2c7a0123e8f5429
sio:SIO_000628
miriam-gene:4255
,
lld:C2939419
;
a
sio:SIO_001121
.
}
dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_provenance
{
dgn-np:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_assertion
dcterms:description
"[Intratumor heterogeneity for expression of P16INK4a and MGMT may reflect intratumor heterogeneity for methylation patterns and thereby in general explain the moderate sensitivity of our marker panel for detection of metastases.]. 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:22266550
;
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:NP582736.RAlxJivrI5b8Ji0kiICTp99kD_u49yJI17tzBrJgkVAxQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:51+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" .
}