@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP169443.RAWwxAdf6BN36cv1FMrqS_pDjBbqQcsPZNzMaM5pq1LqI
> .
@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:NP169443.RAWwxAdf6BN36cv1FMrqS_pDjBbqQcsPZNzMaM5pq1LqI130_head
{
this:
np:hasAssertion
dgn-np:NP169443.RAWwxAdf6BN36cv1FMrqS_pDjBbqQcsPZNzMaM5pq1LqI130_assertion
;
np:hasProvenance
dgn-np:NP169443.RAWwxAdf6BN36cv1FMrqS_pDjBbqQcsPZNzMaM5pq1LqI130_provenance
;
np:hasPublicationInfo
dgn-np:NP169443.RAWwxAdf6BN36cv1FMrqS_pDjBbqQcsPZNzMaM5pq1LqI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP169443.RAWwxAdf6BN36cv1FMrqS_pDjBbqQcsPZNzMaM5pq1LqI130_assertion
a
np:Assertion
.
dgn-np:NP169443.RAWwxAdf6BN36cv1FMrqS_pDjBbqQcsPZNzMaM5pq1LqI130_provenance
a
np:Provenance
.
dgn-np:NP169443.RAWwxAdf6BN36cv1FMrqS_pDjBbqQcsPZNzMaM5pq1LqI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP169443.RAWwxAdf6BN36cv1FMrqS_pDjBbqQcsPZNzMaM5pq1LqI130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN97215e050d733f442bc5d715f0253d05
sio:SIO_000628
miriam-gene:5728
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP169443.RAWwxAdf6BN36cv1FMrqS_pDjBbqQcsPZNzMaM5pq1LqI130_provenance
{
dgn-np:NP169443.RAWwxAdf6BN36cv1FMrqS_pDjBbqQcsPZNzMaM5pq1LqI130_assertion
dcterms:description
"[The PTEN/MMAC1/TEP (PTEN) tumor suppressor gene at 10q23.3 is mutated in multiple types of sporadic tumors including breast cancers and also in the germline of patients with the Cowden's breast cancer predisposition syndrome.]. 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:10597304
;
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:NP169443.RAWwxAdf6BN36cv1FMrqS_pDjBbqQcsPZNzMaM5pq1LqI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:31+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" .
}