@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP228998.RAw69HJnidLdihYUu5WIYJOWHsd5xuW5sp5I--BmODK34
> .
@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:NP228998.RAw69HJnidLdihYUu5WIYJOWHsd5xuW5sp5I--BmODK34130_head
{
this:
np:hasAssertion
dgn-np:NP228998.RAw69HJnidLdihYUu5WIYJOWHsd5xuW5sp5I--BmODK34130_assertion
;
np:hasProvenance
dgn-np:NP228998.RAw69HJnidLdihYUu5WIYJOWHsd5xuW5sp5I--BmODK34130_provenance
;
np:hasPublicationInfo
dgn-np:NP228998.RAw69HJnidLdihYUu5WIYJOWHsd5xuW5sp5I--BmODK34130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP228998.RAw69HJnidLdihYUu5WIYJOWHsd5xuW5sp5I--BmODK34130_assertion
a
np:Assertion
.
dgn-np:NP228998.RAw69HJnidLdihYUu5WIYJOWHsd5xuW5sp5I--BmODK34130_provenance
a
np:Provenance
.
dgn-np:NP228998.RAw69HJnidLdihYUu5WIYJOWHsd5xuW5sp5I--BmODK34130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP228998.RAw69HJnidLdihYUu5WIYJOWHsd5xuW5sp5I--BmODK34130_assertion
{
miriam-gene:4771
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN9d8af8ebba305222fac73def1ffad61e
sio:SIO_000628
miriam-gene:4771
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP228998.RAw69HJnidLdihYUu5WIYJOWHsd5xuW5sp5I--BmODK34130_provenance
{
dgn-np:NP228998.RAw69HJnidLdihYUu5WIYJOWHsd5xuW5sp5I--BmODK34130_assertion
dcterms:description
"[Furthermore, malignant human tumours seemingly unrelated to the NF2 syndrome, such as malignant melanomas (derived from the neural crest) and malignant mesotheliomas (derived from pleural mesoderm), also frequently have mutations or deletions at the NF2 locus, suggesting a broader role of the NF2 gene in the initiation and progression of human neoplasms.]. 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:8718520
;
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:NP228998.RAw69HJnidLdihYUu5WIYJOWHsd5xuW5sp5I--BmODK34130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:08+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" .
}