@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP177000.RAqX_ZjcEnGWOFaEwp18gMWs-2ACs22NWIR1eZXXPbFRM
> .
@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:NP177000.RAqX_ZjcEnGWOFaEwp18gMWs-2ACs22NWIR1eZXXPbFRM130_head
{
this:
np:hasAssertion
dgn-np:NP177000.RAqX_ZjcEnGWOFaEwp18gMWs-2ACs22NWIR1eZXXPbFRM130_assertion
;
np:hasProvenance
dgn-np:NP177000.RAqX_ZjcEnGWOFaEwp18gMWs-2ACs22NWIR1eZXXPbFRM130_provenance
;
np:hasPublicationInfo
dgn-np:NP177000.RAqX_ZjcEnGWOFaEwp18gMWs-2ACs22NWIR1eZXXPbFRM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP177000.RAqX_ZjcEnGWOFaEwp18gMWs-2ACs22NWIR1eZXXPbFRM130_assertion
a
np:Assertion
.
dgn-np:NP177000.RAqX_ZjcEnGWOFaEwp18gMWs-2ACs22NWIR1eZXXPbFRM130_provenance
a
np:Provenance
.
dgn-np:NP177000.RAqX_ZjcEnGWOFaEwp18gMWs-2ACs22NWIR1eZXXPbFRM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP177000.RAqX_ZjcEnGWOFaEwp18gMWs-2ACs22NWIR1eZXXPbFRM130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0018553
a
ncit:C7057
.
dgn-gda:DGN1d57283b8da24cd472cf73d7f7cc4ee7
sio:SIO_000628
miriam-gene:5728
,
lld:C0018553
;
a
sio:SIO_001121
.
}
dgn-np:NP177000.RAqX_ZjcEnGWOFaEwp18gMWs-2ACs22NWIR1eZXXPbFRM130_provenance
{
dgn-np:NP177000.RAqX_ZjcEnGWOFaEwp18gMWs-2ACs22NWIR1eZXXPbFRM130_assertion
dcterms:description
"[The involvement of PTEN in human mammary oncogenesis has been implicated from studies showing that germline PTEN mutation in Cowden disease predisposes to breast cancer, the frequent loss of heterozygosity at the PTEN locus, and reduced PTEN protein levels in sporadic breast cancers.]. 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:NP177000.RAqX_ZjcEnGWOFaEwp18gMWs-2ACs22NWIR1eZXXPbFRM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:35+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" .
}