@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP925982.RAUTn51sv1SIPvi5izEB5I6LNH-MKDhNXLVwnzxWhEtoU
> .
@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:NP925982.RAUTn51sv1SIPvi5izEB5I6LNH-MKDhNXLVwnzxWhEtoU130_head
{
this:
np:hasAssertion
dgn-np:NP925982.RAUTn51sv1SIPvi5izEB5I6LNH-MKDhNXLVwnzxWhEtoU130_assertion
;
np:hasProvenance
dgn-np:NP925982.RAUTn51sv1SIPvi5izEB5I6LNH-MKDhNXLVwnzxWhEtoU130_provenance
;
np:hasPublicationInfo
dgn-np:NP925982.RAUTn51sv1SIPvi5izEB5I6LNH-MKDhNXLVwnzxWhEtoU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP925982.RAUTn51sv1SIPvi5izEB5I6LNH-MKDhNXLVwnzxWhEtoU130_assertion
a
np:Assertion
.
dgn-np:NP925982.RAUTn51sv1SIPvi5izEB5I6LNH-MKDhNXLVwnzxWhEtoU130_provenance
a
np:Provenance
.
dgn-np:NP925982.RAUTn51sv1SIPvi5izEB5I6LNH-MKDhNXLVwnzxWhEtoU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP925982.RAUTn51sv1SIPvi5izEB5I6LNH-MKDhNXLVwnzxWhEtoU130_assertion
{
miriam-gene:7057
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGN0ba994f3dccfbeb583b7a02e380da5ea
sio:SIO_000628
miriam-gene:7057
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP925982.RAUTn51sv1SIPvi5izEB5I6LNH-MKDhNXLVwnzxWhEtoU130_provenance
{
dgn-np:NP925982.RAUTn51sv1SIPvi5izEB5I6LNH-MKDhNXLVwnzxWhEtoU130_assertion
dcterms:description
"[We have recently described a novel pathway termed CpG island methylator phenotype (CIMP) in CRC, which is characterized by the simultaneous methylation of multiple CpG islands, including several known genes, such as p16, hMLH1, and THBS1.]. 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:10639144
;
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:NP925982.RAUTn51sv1SIPvi5izEB5I6LNH-MKDhNXLVwnzxWhEtoU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:28+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" .
}