@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4
> .
@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:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_head
{
this:
np:hasAssertion
dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_assertion
;
np:hasProvenance
dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_provenance
;
np:hasPublicationInfo
dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_assertion
a
np:Assertion
.
dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_provenance
a
np:Provenance
.
dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGN641030febac0c5e03eb5bb0423033f73
sio:SIO_000628
miriam-gene:3342
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_provenance
{
dgn-np:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_assertion
dcterms:description
"[This study indicates that the frequency of genetic alterations in PC as detected by CGH correlates with clinical outcome, and that losses of DNA from chromosomes 6q and 13q are important events that correlate with tumor progression, with loss of 13q, especially instability of locus 171, also associated with angiogenesis.]. 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:14991865
;
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:NP206773.RAOUWUQOYtLmVUF4NZST0Qomye4CritXz2KPXlKGmtMQ4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:54+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" .
}