@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP806636.RAh6nKOWpZeRllkh665OY3FItGWhrbvEgaYtJSITU28JU
> .
@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:NP806636.RAh6nKOWpZeRllkh665OY3FItGWhrbvEgaYtJSITU28JU130_head
{
this:
np:hasAssertion
dgn-np:NP806636.RAh6nKOWpZeRllkh665OY3FItGWhrbvEgaYtJSITU28JU130_assertion
;
np:hasProvenance
dgn-np:NP806636.RAh6nKOWpZeRllkh665OY3FItGWhrbvEgaYtJSITU28JU130_provenance
;
np:hasPublicationInfo
dgn-np:NP806636.RAh6nKOWpZeRllkh665OY3FItGWhrbvEgaYtJSITU28JU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP806636.RAh6nKOWpZeRllkh665OY3FItGWhrbvEgaYtJSITU28JU130_assertion
a
np:Assertion
.
dgn-np:NP806636.RAh6nKOWpZeRllkh665OY3FItGWhrbvEgaYtJSITU28JU130_provenance
a
np:Provenance
.
dgn-np:NP806636.RAh6nKOWpZeRllkh665OY3FItGWhrbvEgaYtJSITU28JU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP806636.RAh6nKOWpZeRllkh665OY3FItGWhrbvEgaYtJSITU28JU130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGNacc6352d42dedc4a3f9923dcd1df071f
sio:SIO_000628
miriam-gene:672
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP806636.RAh6nKOWpZeRllkh665OY3FItGWhrbvEgaYtJSITU28JU130_provenance
{
dgn-np:NP806636.RAh6nKOWpZeRllkh665OY3FItGWhrbvEgaYtJSITU28JU130_assertion
dcterms:description
"[This approach has identified two genetic variants that are associated with colorectal cancer risk in Lynch Syndrome, and five polymorphisms that are associated with the risk of breast cancer for BRCA1 and/or BRCA2 mutation carriers.]. 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:20399636
;
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:NP806636.RAh6nKOWpZeRllkh665OY3FItGWhrbvEgaYtJSITU28JU130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:50+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" .
}