@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP825178.RAyRuiBsSH04uDvIij-bWu2e4-R7f4vFE49Q_K-ihffNg
> .
@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:NP825178.RAyRuiBsSH04uDvIij-bWu2e4-R7f4vFE49Q_K-ihffNg130_head
{
this:
np:hasAssertion
dgn-np:NP825178.RAyRuiBsSH04uDvIij-bWu2e4-R7f4vFE49Q_K-ihffNg130_assertion
;
np:hasProvenance
dgn-np:NP825178.RAyRuiBsSH04uDvIij-bWu2e4-R7f4vFE49Q_K-ihffNg130_provenance
;
np:hasPublicationInfo
dgn-np:NP825178.RAyRuiBsSH04uDvIij-bWu2e4-R7f4vFE49Q_K-ihffNg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP825178.RAyRuiBsSH04uDvIij-bWu2e4-R7f4vFE49Q_K-ihffNg130_assertion
a
np:Assertion
.
dgn-np:NP825178.RAyRuiBsSH04uDvIij-bWu2e4-R7f4vFE49Q_K-ihffNg130_provenance
a
np:Provenance
.
dgn-np:NP825178.RAyRuiBsSH04uDvIij-bWu2e4-R7f4vFE49Q_K-ihffNg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP825178.RAyRuiBsSH04uDvIij-bWu2e4-R7f4vFE49Q_K-ihffNg130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0345967
a
ncit:C7057
.
dgn-gda:DGN667bcc16dbfe978983c3f4cfb2c6b41f
sio:SIO_000628
miriam-gene:3342
,
lld:C0345967
;
a
sio:SIO_001121
.
}
dgn-np:NP825178.RAyRuiBsSH04uDvIij-bWu2e4-R7f4vFE49Q_K-ihffNg130_provenance
{
dgn-np:NP825178.RAyRuiBsSH04uDvIij-bWu2e4-R7f4vFE49Q_K-ihffNg130_assertion
dcterms:description
"[Previous molecular cytogenetic studies by comparative genomic hybridization (CGH) on primary tumours of human malignant mesothelioma have revealed that loss of genetic material at chromosome 14q is one of the most frequently occurring aberrations.]. 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:10584869
;
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:NP825178.RAyRuiBsSH04uDvIij-bWu2e4-R7f4vFE49Q_K-ihffNg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:25+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" .
}