@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP957689.RAfR4IAyIevFhxLi8Do8LxAPQlw-CgC9u2y7NJvMIMoHk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP957689.RAfR4IAyIevFhxLi8Do8LxAPQlw-CgC9u2y7NJvMIMoHk130_head
{
this:
np:hasAssertion
dgn-np:NP957689.RAfR4IAyIevFhxLi8Do8LxAPQlw-CgC9u2y7NJvMIMoHk130_assertion
;
np:hasProvenance
dgn-np:NP957689.RAfR4IAyIevFhxLi8Do8LxAPQlw-CgC9u2y7NJvMIMoHk130_provenance
;
np:hasPublicationInfo
dgn-np:NP957689.RAfR4IAyIevFhxLi8Do8LxAPQlw-CgC9u2y7NJvMIMoHk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP957689.RAfR4IAyIevFhxLi8Do8LxAPQlw-CgC9u2y7NJvMIMoHk130_assertion
a
np:Assertion
.
dgn-np:NP957689.RAfR4IAyIevFhxLi8Do8LxAPQlw-CgC9u2y7NJvMIMoHk130_provenance
a
np:Provenance
.
dgn-np:NP957689.RAfR4IAyIevFhxLi8Do8LxAPQlw-CgC9u2y7NJvMIMoHk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP957689.RAfR4IAyIevFhxLi8Do8LxAPQlw-CgC9u2y7NJvMIMoHk130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNff5044ae498ea95b51e7ff7f7022dac9
sio:SIO_000628
miriam-gene:324
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP957689.RAfR4IAyIevFhxLi8Do8LxAPQlw-CgC9u2y7NJvMIMoHk130_provenance
{
dgn-np:NP957689.RAfR4IAyIevFhxLi8Do8LxAPQlw-CgC9u2y7NJvMIMoHk130_assertion
dcterms:description
"[The underlying propensity for mutation at the APC gene is intriguing, while the greater frequency of mutation in cells defective for DNA repair has relevance to understanding events leading to colorectal cancer and other malignancies.]. 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:22294772
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP957689.RAfR4IAyIevFhxLi8Do8LxAPQlw-CgC9u2y7NJvMIMoHk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:59+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}