@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA
> .
@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:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_head
{
this:
np:hasAssertion
dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_assertion
;
np:hasProvenance
dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_provenance
;
np:hasPublicationInfo
dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_assertion
a
np:Assertion
.
dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_provenance
a
np:Provenance
.
dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_assertion
{
miriam-gene:4771
a
ncit:C16612
.
lld:C0205834
a
ncit:C7057
.
dgn-gda:DGNf9e05896ce006d23e9b7ab032685a28f
sio:SIO_000628
miriam-gene:4771
,
lld:C0205834
;
a
sio:SIO_001121
.
}
dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_provenance
{
dgn-np:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_assertion
dcterms:description
"[Most of these cases display NF2 gene mutations parallel to loss of the chromosome 22 homolog, indicating that inactivation of this gene may represent an early event in the development of multiple meningiomas.]. 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:11979381
;
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:NP471292.RAz3ZCeOA6kAdKxbYguA_Krx5bozy9ksERtpve2_cCpDA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:42+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" .
}