@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g
> .
@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:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_head
{
this:
np:hasAssertion
dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_assertion
;
np:hasProvenance
dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_provenance
;
np:hasPublicationInfo
dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_assertion
a
np:Assertion
.
dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_provenance
a
np:Provenance
.
dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_assertion
{
miriam-gene:4771
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN72a0df67296c02c256b6f5bfc311dcdc
sio:SIO_000628
miriam-gene:4771
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_provenance
{
dgn-np:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_assertion
dcterms:description
"[As the molecular pathogenesis of meningiomas and schwannomas, characterized by NF2 gene alterations, remains unclear and suitable molecular targets need to be identified, we used low density cDNA microarrays to establish expression patterns of 96 cancer-related genes on 23 schwannomas, 42 meningiomas and 3 normal cerebral meninges.]. 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:19148485
;
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:NP786960.RA-wLLTT309TtNtzfnYFRCpz_JLvTZqUrGQl8FvE1WB6g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:00+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" .
}