@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP796772.RABRvf5N70IBeKo1rAwKQdUIqJQzqbE3nLp2Vx3M_ObGY
> .
@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:NP796772.RABRvf5N70IBeKo1rAwKQdUIqJQzqbE3nLp2Vx3M_ObGY130_head
{
this:
np:hasAssertion
dgn-np:NP796772.RABRvf5N70IBeKo1rAwKQdUIqJQzqbE3nLp2Vx3M_ObGY130_assertion
;
np:hasProvenance
dgn-np:NP796772.RABRvf5N70IBeKo1rAwKQdUIqJQzqbE3nLp2Vx3M_ObGY130_provenance
;
np:hasPublicationInfo
dgn-np:NP796772.RABRvf5N70IBeKo1rAwKQdUIqJQzqbE3nLp2Vx3M_ObGY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP796772.RABRvf5N70IBeKo1rAwKQdUIqJQzqbE3nLp2Vx3M_ObGY130_assertion
a
np:Assertion
.
dgn-np:NP796772.RABRvf5N70IBeKo1rAwKQdUIqJQzqbE3nLp2Vx3M_ObGY130_provenance
a
np:Provenance
.
dgn-np:NP796772.RABRvf5N70IBeKo1rAwKQdUIqJQzqbE3nLp2Vx3M_ObGY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP796772.RABRvf5N70IBeKo1rAwKQdUIqJQzqbE3nLp2Vx3M_ObGY130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0032584
a
ncit:C7057
.
dgn-gda:DGN07637a7821fb4e833e7b357863d5e8c3
sio:SIO_000628
miriam-gene:5728
,
lld:C0032584
;
a
sio:SIO_001121
.
}
dgn-np:NP796772.RABRvf5N70IBeKo1rAwKQdUIqJQzqbE3nLp2Vx3M_ObGY130_provenance
{
dgn-np:NP796772.RABRvf5N70IBeKo1rAwKQdUIqJQzqbE3nLp2Vx3M_ObGY130_assertion
dcterms:description
"[This study is the first to show that the mutational abrogation of PTEN/MMAC1 plays a causal role in the genesis of gastrointestinal polyps in Cowden disease, providing molecular genetic evidence that colonic adenoma, juvenile polyp, and gastric hamartoma could be included in the manifestations of Cowden disease.]. 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:9797362
;
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:NP796772.RABRvf5N70IBeKo1rAwKQdUIqJQzqbE3nLp2Vx3M_ObGY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:09+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" .
}