@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP252713.RAH3wcE_IOCLAYnsG2-tgPW6wYQ33V3C6mlbZ8NktW4mI
> .
@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:NP252713.RAH3wcE_IOCLAYnsG2-tgPW6wYQ33V3C6mlbZ8NktW4mI130_head
{
this:
np:hasAssertion
dgn-np:NP252713.RAH3wcE_IOCLAYnsG2-tgPW6wYQ33V3C6mlbZ8NktW4mI130_assertion
;
np:hasProvenance
dgn-np:NP252713.RAH3wcE_IOCLAYnsG2-tgPW6wYQ33V3C6mlbZ8NktW4mI130_provenance
;
np:hasPublicationInfo
dgn-np:NP252713.RAH3wcE_IOCLAYnsG2-tgPW6wYQ33V3C6mlbZ8NktW4mI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP252713.RAH3wcE_IOCLAYnsG2-tgPW6wYQ33V3C6mlbZ8NktW4mI130_assertion
a
np:Assertion
.
dgn-np:NP252713.RAH3wcE_IOCLAYnsG2-tgPW6wYQ33V3C6mlbZ8NktW4mI130_provenance
a
np:Provenance
.
dgn-np:NP252713.RAH3wcE_IOCLAYnsG2-tgPW6wYQ33V3C6mlbZ8NktW4mI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP252713.RAH3wcE_IOCLAYnsG2-tgPW6wYQ33V3C6mlbZ8NktW4mI130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGN513e66e12ad7748d2218da967915c130
sio:SIO_000628
miriam-gene:5728
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP252713.RAH3wcE_IOCLAYnsG2-tgPW6wYQ33V3C6mlbZ8NktW4mI130_provenance
{
dgn-np:NP252713.RAH3wcE_IOCLAYnsG2-tgPW6wYQ33V3C6mlbZ8NktW4mI130_assertion
dcterms:description
"[Although the exact role of germline PTEN mutations in the carcinogenesis of colorectal cancer remains unclear, we think that Cowden syndrome should be in the differential diagnosis of colorectal cancer certainly in view of the possible prognostic and therapeutic consequences.]. 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:21291452
;
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:NP252713.RAH3wcE_IOCLAYnsG2-tgPW6wYQ33V3C6mlbZ8NktW4mI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:21+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" .
}