@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP222796.RAVgUcaNoewLUI3IpjGR6oMOrgcGEIsV-grdzfxDDmgWo
> .
@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:NP222796.RAVgUcaNoewLUI3IpjGR6oMOrgcGEIsV-grdzfxDDmgWo130_head
{
this:
np:hasAssertion
dgn-np:NP222796.RAVgUcaNoewLUI3IpjGR6oMOrgcGEIsV-grdzfxDDmgWo130_assertion
;
np:hasProvenance
dgn-np:NP222796.RAVgUcaNoewLUI3IpjGR6oMOrgcGEIsV-grdzfxDDmgWo130_provenance
;
np:hasPublicationInfo
dgn-np:NP222796.RAVgUcaNoewLUI3IpjGR6oMOrgcGEIsV-grdzfxDDmgWo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP222796.RAVgUcaNoewLUI3IpjGR6oMOrgcGEIsV-grdzfxDDmgWo130_assertion
a
np:Assertion
.
dgn-np:NP222796.RAVgUcaNoewLUI3IpjGR6oMOrgcGEIsV-grdzfxDDmgWo130_provenance
a
np:Provenance
.
dgn-np:NP222796.RAVgUcaNoewLUI3IpjGR6oMOrgcGEIsV-grdzfxDDmgWo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP222796.RAVgUcaNoewLUI3IpjGR6oMOrgcGEIsV-grdzfxDDmgWo130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C1321898
a
ncit:C7057
.
dgn-gda:DGN2d590b79e10b56af9246191514eec793
sio:SIO_000628
miriam-gene:324
,
lld:C1321898
;
a
sio:SIO_001121
.
}
dgn-np:NP222796.RAVgUcaNoewLUI3IpjGR6oMOrgcGEIsV-grdzfxDDmgWo130_provenance
{
dgn-np:NP222796.RAVgUcaNoewLUI3IpjGR6oMOrgcGEIsV-grdzfxDDmgWo130_assertion
dcterms:description
"[Familial adenomatous polyposis (FAP), hereditary nonpolyposis colorectal cancer (HNPCC), as well as early stages of spontaneous CRC, can be diagnosed by molecular characterisation of the adenomatous polyposis coli (APC) gene, the RAS oncogene and other genes in DNA from peripheral blood, stool or intestinal biopsies.]. 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:7577053
;
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:NP222796.RAVgUcaNoewLUI3IpjGR6oMOrgcGEIsV-grdzfxDDmgWo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:03+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" .
}