@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP468372.RAYprY8h2ZN6GlK3tfP7tXOB-JHTtCF9QDeM1m5A47zWw
> .
@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:NP468372.RAYprY8h2ZN6GlK3tfP7tXOB-JHTtCF9QDeM1m5A47zWw130_head
{
this:
np:hasAssertion
dgn-np:NP468372.RAYprY8h2ZN6GlK3tfP7tXOB-JHTtCF9QDeM1m5A47zWw130_assertion
;
np:hasProvenance
dgn-np:NP468372.RAYprY8h2ZN6GlK3tfP7tXOB-JHTtCF9QDeM1m5A47zWw130_provenance
;
np:hasPublicationInfo
dgn-np:NP468372.RAYprY8h2ZN6GlK3tfP7tXOB-JHTtCF9QDeM1m5A47zWw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP468372.RAYprY8h2ZN6GlK3tfP7tXOB-JHTtCF9QDeM1m5A47zWw130_assertion
a
np:Assertion
.
dgn-np:NP468372.RAYprY8h2ZN6GlK3tfP7tXOB-JHTtCF9QDeM1m5A47zWw130_provenance
a
np:Provenance
.
dgn-np:NP468372.RAYprY8h2ZN6GlK3tfP7tXOB-JHTtCF9QDeM1m5A47zWw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP468372.RAYprY8h2ZN6GlK3tfP7tXOB-JHTtCF9QDeM1m5A47zWw130_assertion
{
miriam-gene:29974
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN22f408db069dc366b08841c73d6966be
sio:SIO_000628
miriam-gene:29974
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP468372.RAYprY8h2ZN6GlK3tfP7tXOB-JHTtCF9QDeM1m5A47zWw130_provenance
{
dgn-np:NP468372.RAYprY8h2ZN6GlK3tfP7tXOB-JHTtCF9QDeM1m5A47zWw130_assertion
dcterms:description
"[The aims of this study are to characterize the frequency, density, and distribution of aberrant crypt foci (ACF) and its histological features and to determine the frequency of loss of expression of DNA mismatch repair (MMR) proteins of subjects with hereditary nonpolyposic colorectal cancer (HNPCC) and sporadic colon rectal cancer (CRC).]. 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:21744313
;
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:NP468372.RAYprY8h2ZN6GlK3tfP7tXOB-JHTtCF9QDeM1m5A47zWw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:41+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" .
}