@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP208369.RAHw3NMpzXuRpWABMBThlvMZWQGHMNh4FvZHHgJ-3cQD0
> .
@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:NP208369.RAHw3NMpzXuRpWABMBThlvMZWQGHMNh4FvZHHgJ-3cQD0130_head
{
this:
np:hasAssertion
dgn-np:NP208369.RAHw3NMpzXuRpWABMBThlvMZWQGHMNh4FvZHHgJ-3cQD0130_assertion
;
np:hasProvenance
dgn-np:NP208369.RAHw3NMpzXuRpWABMBThlvMZWQGHMNh4FvZHHgJ-3cQD0130_provenance
;
np:hasPublicationInfo
dgn-np:NP208369.RAHw3NMpzXuRpWABMBThlvMZWQGHMNh4FvZHHgJ-3cQD0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP208369.RAHw3NMpzXuRpWABMBThlvMZWQGHMNh4FvZHHgJ-3cQD0130_assertion
a
np:Assertion
.
dgn-np:NP208369.RAHw3NMpzXuRpWABMBThlvMZWQGHMNh4FvZHHgJ-3cQD0130_provenance
a
np:Provenance
.
dgn-np:NP208369.RAHw3NMpzXuRpWABMBThlvMZWQGHMNh4FvZHHgJ-3cQD0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP208369.RAHw3NMpzXuRpWABMBThlvMZWQGHMNh4FvZHHgJ-3cQD0130_assertion
{
miriam-gene:4771
a
ncit:C16612
.
lld:C0025286
a
ncit:C7057
.
dgn-gda:DGN7968ccd03ff961c75c7149c0b6cb6cea
sio:SIO_000628
miriam-gene:4771
,
lld:C0025286
;
a
sio:SIO_001121
.
}
dgn-np:NP208369.RAHw3NMpzXuRpWABMBThlvMZWQGHMNh4FvZHHgJ-3cQD0130_provenance
{
dgn-np:NP208369.RAHw3NMpzXuRpWABMBThlvMZWQGHMNh4FvZHHgJ-3cQD0130_assertion
dcterms:description
"[These data strongly support the notion that NF2 is the sole target of 22q LOH in meningiomas and that loss of merlin expression is always caused by genetic alteration of NF2, following the classic `two hit` theory.]. 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:10606247
;
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:NP208369.RAHw3NMpzXuRpWABMBThlvMZWQGHMNh4FvZHHgJ-3cQD0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:55+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" .
}