@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E
> .
@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:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_head
{
this:
np:hasAssertion
dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_assertion
;
np:hasProvenance
dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_provenance
;
np:hasPublicationInfo
dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_assertion
a
np:Assertion
.
dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_provenance
a
np:Provenance
.
dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_assertion
{
miriam-gene:4771
a
ncit:C16612
.
lld:C0085136
a
ncit:C7057
.
dgn-gda:DGNb0e4424fc70f2f5a10a0cd24b0600885
sio:SIO_000628
miriam-gene:4771
,
lld:C0085136
;
a
sio:SIO_001121
.
}
dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_provenance
{
dgn-np:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_assertion
dcterms:description
"[Mutations of the neurofibromatosis 2 (NF2) tumor suppressor gene have frequently been detected not only in schwannomas and other central nervous system tumors of NF2 patients but also in their sporadic counterparts and malignant tumors unrelated to the NF2 syndrome such as malignant mesothelioma, indicating a broader role for the NF2 gene in human 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:17210637
;
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:NP676263.RA4gNd3W_SBmm7NNXlM0JuZc4hwAb0Q7pb_fvf8OVFp2E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:48+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" .
}