@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP437203.RAmtSVtPVt28r67Y64RQBbews_0bURblQvBva02ufTSiI
> .
@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:NP437203.RAmtSVtPVt28r67Y64RQBbews_0bURblQvBva02ufTSiI130_head
{
this:
np:hasAssertion
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;
np:hasProvenance
dgn-np:NP437203.RAmtSVtPVt28r67Y64RQBbews_0bURblQvBva02ufTSiI130_provenance
;
np:hasPublicationInfo
dgn-np:NP437203.RAmtSVtPVt28r67Y64RQBbews_0bURblQvBva02ufTSiI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP437203.RAmtSVtPVt28r67Y64RQBbews_0bURblQvBva02ufTSiI130_assertion
a
np:Assertion
.
dgn-np:NP437203.RAmtSVtPVt28r67Y64RQBbews_0bURblQvBva02ufTSiI130_provenance
a
np:Provenance
.
dgn-np:NP437203.RAmtSVtPVt28r67Y64RQBbews_0bURblQvBva02ufTSiI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP437203.RAmtSVtPVt28r67Y64RQBbews_0bURblQvBva02ufTSiI130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0001418
a
ncit:C7057
.
dgn-gda:DGN8c5a668bafe0ec2ab24b9d6e463e53d5
sio:SIO_000628
miriam-gene:7248
,
lld:C0001418
;
a
sio:SIO_001121
.
}
dgn-np:NP437203.RAmtSVtPVt28r67Y64RQBbews_0bURblQvBva02ufTSiI130_provenance
{
dgn-np:NP437203.RAmtSVtPVt28r67Y64RQBbews_0bURblQvBva02ufTSiI130_assertion
dcterms:description
"[We conclude that LOH at chromosome 10q23 is uncommon in BOAd, is not associated with mutations in the PTEN tumour suppressor gene, and does not correlate with the clinical or pathologic features of these tumours.]. 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:11259087
;
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:NP437203.RAmtSVtPVt28r67Y64RQBbews_0bURblQvBva02ufTSiI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:19+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" .
}