@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP754208.RAaGjl-b9y1h5KzMkCXTqXZy098zGEJHZDj_egjiNSA9M
> .
@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:NP754208.RAaGjl-b9y1h5KzMkCXTqXZy098zGEJHZDj_egjiNSA9M130_head
{
this:
np:hasAssertion
dgn-np:NP754208.RAaGjl-b9y1h5KzMkCXTqXZy098zGEJHZDj_egjiNSA9M130_assertion
;
np:hasProvenance
dgn-np:NP754208.RAaGjl-b9y1h5KzMkCXTqXZy098zGEJHZDj_egjiNSA9M130_provenance
;
np:hasPublicationInfo
dgn-np:NP754208.RAaGjl-b9y1h5KzMkCXTqXZy098zGEJHZDj_egjiNSA9M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP754208.RAaGjl-b9y1h5KzMkCXTqXZy098zGEJHZDj_egjiNSA9M130_assertion
a
np:Assertion
.
dgn-np:NP754208.RAaGjl-b9y1h5KzMkCXTqXZy098zGEJHZDj_egjiNSA9M130_provenance
a
np:Provenance
.
dgn-np:NP754208.RAaGjl-b9y1h5KzMkCXTqXZy098zGEJHZDj_egjiNSA9M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP754208.RAaGjl-b9y1h5KzMkCXTqXZy098zGEJHZDj_egjiNSA9M130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0027672
a
ncit:C7057
.
dgn-gda:DGN04fd52326e7acf44569dac758a61ffa6
sio:SIO_000628
miriam-gene:5728
,
lld:C0027672
;
a
sio:SIO_001121
.
}
dgn-np:NP754208.RAaGjl-b9y1h5KzMkCXTqXZy098zGEJHZDj_egjiNSA9M130_provenance
{
dgn-np:NP754208.RAaGjl-b9y1h5KzMkCXTqXZy098zGEJHZDj_egjiNSA9M130_assertion
dcterms:description
"[Allele loss close to the PTEN locus occurs in sporadic colon cancer and germline PTEN mutations cause Cowden disease, an inherited cancer syndrome characterized by an increased incidence of gastrointestinal tract lesions that can progress to colorectal carcinoma.]. 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:11439367
;
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:NP754208.RAaGjl-b9y1h5KzMkCXTqXZy098zGEJHZDj_egjiNSA9M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:37+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" .
}