@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_head
{
this:
np:hasAssertion
dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_assertion
;
np:hasProvenance
dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_provenance
;
np:hasPublicationInfo
dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_assertion
a
np:Assertion
.
dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_provenance
a
np:Provenance
.
dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_assertion
{
miriam-gene:4763
a
ncit:C16612
.
lld:C0751690
a
ncit:C7057
.
dgn-gda:DGN2377426fedd4c74eea83d600d61285ae
sio:SIO_000628
miriam-gene:4763
,
lld:C0751690
;
a
sio:SIO_001121
.
}
dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_provenance
{
dgn-np:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_assertion
dcterms:description
"[This study suggests that the germline mutation in one of the copies accompanied by loss or inactivation of the second copy of the NF1 gene and tumor suppressor gene(s) on 17p and 22q may be associated with the neoplastic transformation; abnormalities of other chromosomes may be related to progression of MPNST.]. 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:7828144
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1323093.RAhiCHUBA7reWLg6_cjfHKhbhjtlj7t6VpFOmI4NzkjUI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:46+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}