@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP474924.RAksL-h_XBKwJr57wv-6ycs1pdXvPFI1NsWfErgRF5K3I
> .
@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:NP474924.RAksL-h_XBKwJr57wv-6ycs1pdXvPFI1NsWfErgRF5K3I130_head
{
this:
np:hasAssertion
dgn-np:NP474924.RAksL-h_XBKwJr57wv-6ycs1pdXvPFI1NsWfErgRF5K3I130_assertion
;
np:hasProvenance
dgn-np:NP474924.RAksL-h_XBKwJr57wv-6ycs1pdXvPFI1NsWfErgRF5K3I130_provenance
;
np:hasPublicationInfo
dgn-np:NP474924.RAksL-h_XBKwJr57wv-6ycs1pdXvPFI1NsWfErgRF5K3I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP474924.RAksL-h_XBKwJr57wv-6ycs1pdXvPFI1NsWfErgRF5K3I130_assertion
a
np:Assertion
.
dgn-np:NP474924.RAksL-h_XBKwJr57wv-6ycs1pdXvPFI1NsWfErgRF5K3I130_provenance
a
np:Provenance
.
dgn-np:NP474924.RAksL-h_XBKwJr57wv-6ycs1pdXvPFI1NsWfErgRF5K3I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP474924.RAksL-h_XBKwJr57wv-6ycs1pdXvPFI1NsWfErgRF5K3I130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN1cb9b870d92a5f971f2d45fd1706d6aa
sio:SIO_000628
miriam-gene:1029
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP474924.RAksL-h_XBKwJr57wv-6ycs1pdXvPFI1NsWfErgRF5K3I130_provenance
{
dgn-np:NP474924.RAksL-h_XBKwJr57wv-6ycs1pdXvPFI1NsWfErgRF5K3I130_assertion
dcterms:description
"[In this study, 30 commonly used CRC cell lines as well as seven primary tumours from individuals with hereditary nonpolyposis colorectal cancer (HNPCC) were assessed for methylation at six CpG islands known to be hypermethylated in colorectal cancer: hMLH1, p16, methylated in tumour (MINT-)-1, -2, -12 and -31.]. 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:12569385
;
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:NP474924.RAksL-h_XBKwJr57wv-6ycs1pdXvPFI1NsWfErgRF5K3I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:44+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" .
}