@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP487685.RAoOgopMhikvhXtVLdAS44fJ6T03B5MweZ6epccasN144
> .
@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:NP487685.RAoOgopMhikvhXtVLdAS44fJ6T03B5MweZ6epccasN144130_head
{
this:
np:hasAssertion
dgn-np:NP487685.RAoOgopMhikvhXtVLdAS44fJ6T03B5MweZ6epccasN144130_assertion
;
np:hasProvenance
dgn-np:NP487685.RAoOgopMhikvhXtVLdAS44fJ6T03B5MweZ6epccasN144130_provenance
;
np:hasPublicationInfo
dgn-np:NP487685.RAoOgopMhikvhXtVLdAS44fJ6T03B5MweZ6epccasN144130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP487685.RAoOgopMhikvhXtVLdAS44fJ6T03B5MweZ6epccasN144130_assertion
a
np:Assertion
.
dgn-np:NP487685.RAoOgopMhikvhXtVLdAS44fJ6T03B5MweZ6epccasN144130_provenance
a
np:Provenance
.
dgn-np:NP487685.RAoOgopMhikvhXtVLdAS44fJ6T03B5MweZ6epccasN144130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP487685.RAoOgopMhikvhXtVLdAS44fJ6T03B5MweZ6epccasN144130_assertion
{
miriam-gene:8731
a
ncit:C16612
.
lld:C0007134
a
ncit:C7057
.
dgn-gda:DGN0c00676c1ccf98fccf1096a8417ca48b
sio:SIO_000628
miriam-gene:8731
,
lld:C0007134
;
a
sio:SIO_001121
.
}
dgn-np:NP487685.RAoOgopMhikvhXtVLdAS44fJ6T03B5MweZ6epccasN144130_provenance
{
dgn-np:NP487685.RAoOgopMhikvhXtVLdAS44fJ6T03B5MweZ6epccasN144130_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:NP487685.RAoOgopMhikvhXtVLdAS44fJ6T03B5MweZ6epccasN144130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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" .
}