@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP316603.RAlU1iMLZpsY1M4_0EMnJg2AmIMPy9z3rVoS7hiF0beNA
> .
@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:NP316603.RAlU1iMLZpsY1M4_0EMnJg2AmIMPy9z3rVoS7hiF0beNA130_head
{
this:
np:hasAssertion
dgn-np:NP316603.RAlU1iMLZpsY1M4_0EMnJg2AmIMPy9z3rVoS7hiF0beNA130_assertion
;
np:hasProvenance
dgn-np:NP316603.RAlU1iMLZpsY1M4_0EMnJg2AmIMPy9z3rVoS7hiF0beNA130_provenance
;
np:hasPublicationInfo
dgn-np:NP316603.RAlU1iMLZpsY1M4_0EMnJg2AmIMPy9z3rVoS7hiF0beNA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP316603.RAlU1iMLZpsY1M4_0EMnJg2AmIMPy9z3rVoS7hiF0beNA130_assertion
a
np:Assertion
.
dgn-np:NP316603.RAlU1iMLZpsY1M4_0EMnJg2AmIMPy9z3rVoS7hiF0beNA130_provenance
a
np:Provenance
.
dgn-np:NP316603.RAlU1iMLZpsY1M4_0EMnJg2AmIMPy9z3rVoS7hiF0beNA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP316603.RAlU1iMLZpsY1M4_0EMnJg2AmIMPy9z3rVoS7hiF0beNA130_assertion
{
miriam-gene:4856
a
ncit:C16612
.
lld:C0684743
a
ncit:C7057
.
dgn-gda:DGN742a12a2fd9964784d053d165263dcca
sio:SIO_000628
miriam-gene:4856
,
lld:C0684743
;
a
sio:SIO_001121
.
}
dgn-np:NP316603.RAlU1iMLZpsY1M4_0EMnJg2AmIMPy9z3rVoS7hiF0beNA130_provenance
{
dgn-np:NP316603.RAlU1iMLZpsY1M4_0EMnJg2AmIMPy9z3rVoS7hiF0beNA130_assertion
dcterms:description
"[Elevated expression of the CCN3 (also known as NOV, Nephroblastoma overexpressed) gene has been detected in clinical samples of the skeletal muscle cancer rhabdomyosarcoma, with the highest expression found in the alveolar subtype (aRMS).]. 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:21423212
;
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:NP316603.RAlU1iMLZpsY1M4_0EMnJg2AmIMPy9z3rVoS7hiF0beNA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:03+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" .
}