@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47797.RAA_eFgIsT3pXzH2X_E38SHMcAXDtsqE2NCwurCZl61f4
> .
@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:NP47797.RAA_eFgIsT3pXzH2X_E38SHMcAXDtsqE2NCwurCZl61f4130_head
{
this:
np:hasAssertion
dgn-np:NP47797.RAA_eFgIsT3pXzH2X_E38SHMcAXDtsqE2NCwurCZl61f4130_assertion
;
np:hasProvenance
dgn-np:NP47797.RAA_eFgIsT3pXzH2X_E38SHMcAXDtsqE2NCwurCZl61f4130_provenance
;
np:hasPublicationInfo
dgn-np:NP47797.RAA_eFgIsT3pXzH2X_E38SHMcAXDtsqE2NCwurCZl61f4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47797.RAA_eFgIsT3pXzH2X_E38SHMcAXDtsqE2NCwurCZl61f4130_assertion
a
np:Assertion
.
dgn-np:NP47797.RAA_eFgIsT3pXzH2X_E38SHMcAXDtsqE2NCwurCZl61f4130_provenance
a
np:Provenance
.
dgn-np:NP47797.RAA_eFgIsT3pXzH2X_E38SHMcAXDtsqE2NCwurCZl61f4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47797.RAA_eFgIsT3pXzH2X_E38SHMcAXDtsqE2NCwurCZl61f4130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNeaca56420cccc280cc0b41d9fde17a05
sio:SIO_000628
miriam-gene:672
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP47797.RAA_eFgIsT3pXzH2X_E38SHMcAXDtsqE2NCwurCZl61f4130_provenance
{
dgn-np:NP47797.RAA_eFgIsT3pXzH2X_E38SHMcAXDtsqE2NCwurCZl61f4130_assertion
dcterms:description
"[To establish whether or not inherited variation in BRCA1 influences the risk of colorectal cancer, we genotyped 2,398 unselected patients with colorectal cancer and 4,570 controls from Poland for three BRCA1 founder mutations (C61G, 4153delA and 5382insC).]. 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:20862552
;
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:NP47797.RAA_eFgIsT3pXzH2X_E38SHMcAXDtsqE2NCwurCZl61f4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}