@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP809086.RAlVAGUpv1V2pNTv_WZUVtC909CNUpsD-F8SRygLLtgiE
> .
@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:NP809086.RAlVAGUpv1V2pNTv_WZUVtC909CNUpsD-F8SRygLLtgiE130_head
{
this:
np:hasAssertion
dgn-np:NP809086.RAlVAGUpv1V2pNTv_WZUVtC909CNUpsD-F8SRygLLtgiE130_assertion
;
np:hasProvenance
dgn-np:NP809086.RAlVAGUpv1V2pNTv_WZUVtC909CNUpsD-F8SRygLLtgiE130_provenance
;
np:hasPublicationInfo
dgn-np:NP809086.RAlVAGUpv1V2pNTv_WZUVtC909CNUpsD-F8SRygLLtgiE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP809086.RAlVAGUpv1V2pNTv_WZUVtC909CNUpsD-F8SRygLLtgiE130_assertion
a
np:Assertion
.
dgn-np:NP809086.RAlVAGUpv1V2pNTv_WZUVtC909CNUpsD-F8SRygLLtgiE130_provenance
a
np:Provenance
.
dgn-np:NP809086.RAlVAGUpv1V2pNTv_WZUVtC909CNUpsD-F8SRygLLtgiE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP809086.RAlVAGUpv1V2pNTv_WZUVtC909CNUpsD-F8SRygLLtgiE130_assertion
{
miriam-gene:8731
a
ncit:C16612
.
lld:C0041107
a
ncit:C7057
.
dgn-gda:DGN8e5d21307e71b1043a0bb5a633077224
sio:SIO_000628
miriam-gene:8731
,
lld:C0041107
;
a
sio:SIO_001121
.
}
dgn-np:NP809086.RAlVAGUpv1V2pNTv_WZUVtC909CNUpsD-F8SRygLLtgiE130_provenance
{
dgn-np:NP809086.RAlVAGUpv1V2pNTv_WZUVtC909CNUpsD-F8SRygLLtgiE130_assertion
dcterms:description
"[This finding, and that of trisomy 7 and MET mutation in hereditary renal carcinoma represent the only cases of human tumors in which an increased number of chromosomes carrying an oncogene activated by point mutation have been detected.]. 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:10812167
;
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:NP809086.RAlVAGUpv1V2pNTv_WZUVtC909CNUpsD-F8SRygLLtgiE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:16+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" .
}