@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP177570.RAtZVi4m_0dyv48VpsfrsEDQ4WiaB1helbtRCakae9pl8
> .
@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:NP177570.RAtZVi4m_0dyv48VpsfrsEDQ4WiaB1helbtRCakae9pl8130_head
{
this:
np:hasAssertion
dgn-np:NP177570.RAtZVi4m_0dyv48VpsfrsEDQ4WiaB1helbtRCakae9pl8130_assertion
;
np:hasProvenance
dgn-np:NP177570.RAtZVi4m_0dyv48VpsfrsEDQ4WiaB1helbtRCakae9pl8130_provenance
;
np:hasPublicationInfo
dgn-np:NP177570.RAtZVi4m_0dyv48VpsfrsEDQ4WiaB1helbtRCakae9pl8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP177570.RAtZVi4m_0dyv48VpsfrsEDQ4WiaB1helbtRCakae9pl8130_assertion
a
np:Assertion
.
dgn-np:NP177570.RAtZVi4m_0dyv48VpsfrsEDQ4WiaB1helbtRCakae9pl8130_provenance
a
np:Provenance
.
dgn-np:NP177570.RAtZVi4m_0dyv48VpsfrsEDQ4WiaB1helbtRCakae9pl8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP177570.RAtZVi4m_0dyv48VpsfrsEDQ4WiaB1helbtRCakae9pl8130_assertion
{
miriam-gene:1111
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGN282efa63ea49bf920eda3313da30bb26
sio:SIO_000628
miriam-gene:1111
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP177570.RAtZVi4m_0dyv48VpsfrsEDQ4WiaB1helbtRCakae9pl8130_provenance
{
dgn-np:NP177570.RAtZVi4m_0dyv48VpsfrsEDQ4WiaB1helbtRCakae9pl8130_assertion
dcterms:description
"[Our data also suggest that CHK1 deletion is an early genetic event in the development of breast cancer and can be detected at the DCIS stage, whereas CCND1 amplification is more likely to be associated with tumour progression.]. 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:21401699
;
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:NP177570.RAtZVi4m_0dyv48VpsfrsEDQ4WiaB1helbtRCakae9pl8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:36+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" .
}