@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY
> .
@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:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_head
{
this:
np:hasAssertion
dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_assertion
;
np:hasProvenance
dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_provenance
;
np:hasPublicationInfo
dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_assertion
a
np:Assertion
.
dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_provenance
a
np:Provenance
.
dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_assertion
{
miriam-gene:4318
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN7a34091d3777a4dc1a3bc2532bab8744
sio:SIO_000628
miriam-gene:4318
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_provenance
{
dgn-np:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_assertion
dcterms:description
"[Our results indicate that MMP-2 -1306 C/T polymorphism may be associated with genetic susceptibility to colorectal cancer and the invasive capability of colorectal cancer in Chinese patients. And it is easier for the CC genotype cancer to invade through bowel wall.]. 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:16456793
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP65755.RAeEXsXe-pEKckIy04WL5x_jreHc-xrCJrOHGcrmcJEpY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:31+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" .
}