@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP462946.RAuZOBFa8tENTOrAH_xK8nn-qa5Q2DH_bidH968zw5Vyw
> .
@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:NP462946.RAuZOBFa8tENTOrAH_xK8nn-qa5Q2DH_bidH968zw5Vyw130_head
{
this:
np:hasAssertion
dgn-np:NP462946.RAuZOBFa8tENTOrAH_xK8nn-qa5Q2DH_bidH968zw5Vyw130_assertion
;
np:hasProvenance
dgn-np:NP462946.RAuZOBFa8tENTOrAH_xK8nn-qa5Q2DH_bidH968zw5Vyw130_provenance
;
np:hasPublicationInfo
dgn-np:NP462946.RAuZOBFa8tENTOrAH_xK8nn-qa5Q2DH_bidH968zw5Vyw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP462946.RAuZOBFa8tENTOrAH_xK8nn-qa5Q2DH_bidH968zw5Vyw130_assertion
a
np:Assertion
.
dgn-np:NP462946.RAuZOBFa8tENTOrAH_xK8nn-qa5Q2DH_bidH968zw5Vyw130_provenance
a
np:Provenance
.
dgn-np:NP462946.RAuZOBFa8tENTOrAH_xK8nn-qa5Q2DH_bidH968zw5Vyw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP462946.RAuZOBFa8tENTOrAH_xK8nn-qa5Q2DH_bidH968zw5Vyw130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0014170
a
ncit:C7057
.
dgn-gda:DGNde36b86209e27ebfec4d408b2d06a066
sio:SIO_000628
miriam-gene:5728
,
lld:C0014170
;
a
sio:SIO_001121
.
}
dgn-np:NP462946.RAuZOBFa8tENTOrAH_xK8nn-qa5Q2DH_bidH968zw5Vyw130_provenance
{
dgn-np:NP462946.RAuZOBFa8tENTOrAH_xK8nn-qa5Q2DH_bidH968zw5Vyw130_assertion
dcterms:description
"[Loss of heterozygosity using three microsatellites (D10S215, D10S541, and D10S564) and the complete sequence analysis of PTEN exons in breast and endometrial tumor samples from the same patient were also carried out in an attempt to identify additional PTEN somatic mutations.]. 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:14675182
;
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:NP462946.RAuZOBFa8tENTOrAH_xK8nn-qa5Q2DH_bidH968zw5Vyw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:35+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" .
}