@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1179935.RAPwgLlYYo5BBGJ8yc2ZBSXkgxZ9JErNUFM75Wzx_oBoU
> .
@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:NP1179935.RAPwgLlYYo5BBGJ8yc2ZBSXkgxZ9JErNUFM75Wzx_oBoU130_head
{
this:
np:hasAssertion
dgn-np:NP1179935.RAPwgLlYYo5BBGJ8yc2ZBSXkgxZ9JErNUFM75Wzx_oBoU130_assertion
;
np:hasProvenance
dgn-np:NP1179935.RAPwgLlYYo5BBGJ8yc2ZBSXkgxZ9JErNUFM75Wzx_oBoU130_provenance
;
np:hasPublicationInfo
dgn-np:NP1179935.RAPwgLlYYo5BBGJ8yc2ZBSXkgxZ9JErNUFM75Wzx_oBoU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1179935.RAPwgLlYYo5BBGJ8yc2ZBSXkgxZ9JErNUFM75Wzx_oBoU130_assertion
a
np:Assertion
.
dgn-np:NP1179935.RAPwgLlYYo5BBGJ8yc2ZBSXkgxZ9JErNUFM75Wzx_oBoU130_provenance
a
np:Provenance
.
dgn-np:NP1179935.RAPwgLlYYo5BBGJ8yc2ZBSXkgxZ9JErNUFM75Wzx_oBoU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1179935.RAPwgLlYYo5BBGJ8yc2ZBSXkgxZ9JErNUFM75Wzx_oBoU130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN7805b6d69a92cbe7cab2697515844925
sio:SIO_000628
miriam-gene:5624
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP1179935.RAPwgLlYYo5BBGJ8yc2ZBSXkgxZ9JErNUFM75Wzx_oBoU130_provenance
{
dgn-np:NP1179935.RAPwgLlYYo5BBGJ8yc2ZBSXkgxZ9JErNUFM75Wzx_oBoU130_assertion
dcterms:description
"[In FAP patients, the CRC risk score did not differ significantly from the controls, as we expected given the overwhelming effect of pathogenic germline APC variants on the phenotype of these cases.]. 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:24801760
;
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:NP1179935.RAPwgLlYYo5BBGJ8yc2ZBSXkgxZ9JErNUFM75Wzx_oBoU130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:40+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" .
}