@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP191675.RAl4wBD2HWKccL80B7Fl1HUY1vIyJ9W2lBV0ZzSQgnYeI
> .
@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:NP191675.RAl4wBD2HWKccL80B7Fl1HUY1vIyJ9W2lBV0ZzSQgnYeI130_head
{
this:
np:hasAssertion
dgn-np:NP191675.RAl4wBD2HWKccL80B7Fl1HUY1vIyJ9W2lBV0ZzSQgnYeI130_assertion
;
np:hasProvenance
dgn-np:NP191675.RAl4wBD2HWKccL80B7Fl1HUY1vIyJ9W2lBV0ZzSQgnYeI130_provenance
;
np:hasPublicationInfo
dgn-np:NP191675.RAl4wBD2HWKccL80B7Fl1HUY1vIyJ9W2lBV0ZzSQgnYeI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP191675.RAl4wBD2HWKccL80B7Fl1HUY1vIyJ9W2lBV0ZzSQgnYeI130_assertion
a
np:Assertion
.
dgn-np:NP191675.RAl4wBD2HWKccL80B7Fl1HUY1vIyJ9W2lBV0ZzSQgnYeI130_provenance
a
np:Provenance
.
dgn-np:NP191675.RAl4wBD2HWKccL80B7Fl1HUY1vIyJ9W2lBV0ZzSQgnYeI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP191675.RAl4wBD2HWKccL80B7Fl1HUY1vIyJ9W2lBV0ZzSQgnYeI130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0027859
a
ncit:C7057
.
dgn-gda:DGN1eac75807079d112a02c3a1942a43130
sio:SIO_000628
miriam-gene:3342
,
lld:C0027859
;
a
sio:SIO_001121
.
}
dgn-np:NP191675.RAl4wBD2HWKccL80B7Fl1HUY1vIyJ9W2lBV0ZzSQgnYeI130_provenance
{
dgn-np:NP191675.RAl4wBD2HWKccL80B7Fl1HUY1vIyJ9W2lBV0ZzSQgnYeI130_assertion
dcterms:description
"[Comparative genomic hybridisation (CGH) was used to screen 76 vestibular schwannomas from 76 patients (66 sporadic and 10 NF2 related) to identify other chromosome regions that may harbour genes involved in the tumorigenesis.]. 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:14627667
;
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:NP191675.RAl4wBD2HWKccL80B7Fl1HUY1vIyJ9W2lBV0ZzSQgnYeI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:45+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" .
}