@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP220269.RA61M6T3JV75EuCxa1-ZInXHDZPR9ik282oVHTJzx9WiA
> .
@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:NP220269.RA61M6T3JV75EuCxa1-ZInXHDZPR9ik282oVHTJzx9WiA130_head
{
this:
np:hasAssertion
dgn-np:NP220269.RA61M6T3JV75EuCxa1-ZInXHDZPR9ik282oVHTJzx9WiA130_assertion
;
np:hasProvenance
dgn-np:NP220269.RA61M6T3JV75EuCxa1-ZInXHDZPR9ik282oVHTJzx9WiA130_provenance
;
np:hasPublicationInfo
dgn-np:NP220269.RA61M6T3JV75EuCxa1-ZInXHDZPR9ik282oVHTJzx9WiA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP220269.RA61M6T3JV75EuCxa1-ZInXHDZPR9ik282oVHTJzx9WiA130_assertion
a
np:Assertion
.
dgn-np:NP220269.RA61M6T3JV75EuCxa1-ZInXHDZPR9ik282oVHTJzx9WiA130_provenance
a
np:Provenance
.
dgn-np:NP220269.RA61M6T3JV75EuCxa1-ZInXHDZPR9ik282oVHTJzx9WiA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP220269.RA61M6T3JV75EuCxa1-ZInXHDZPR9ik282oVHTJzx9WiA130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN98daa2d599b729b8f798866fe183a8d6
sio:SIO_000628
miriam-gene:5728
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP220269.RA61M6T3JV75EuCxa1-ZInXHDZPR9ik282oVHTJzx9WiA130_provenance
{
dgn-np:NP220269.RA61M6T3JV75EuCxa1-ZInXHDZPR9ik282oVHTJzx9WiA130_assertion
dcterms:description
"[The PTEN gene is often mutated in primary human tumors and cell lines, but the low rate of somatic PTEN mutation in human breast cancer has led to debate over the role of this tumor suppressor in this 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:11737885
;
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:NP220269.RA61M6T3JV75EuCxa1-ZInXHDZPR9ik282oVHTJzx9WiA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:02+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" .
}