@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP283992.RAn-MZE9qFzYpct9pbq22V6SRBZbMVoXbjS4CWBV5r8C8
> .
@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:NP283992.RAn-MZE9qFzYpct9pbq22V6SRBZbMVoXbjS4CWBV5r8C8130_head
{
this:
np:hasAssertion
dgn-np:NP283992.RAn-MZE9qFzYpct9pbq22V6SRBZbMVoXbjS4CWBV5r8C8130_assertion
;
np:hasProvenance
dgn-np:NP283992.RAn-MZE9qFzYpct9pbq22V6SRBZbMVoXbjS4CWBV5r8C8130_provenance
;
np:hasPublicationInfo
dgn-np:NP283992.RAn-MZE9qFzYpct9pbq22V6SRBZbMVoXbjS4CWBV5r8C8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP283992.RAn-MZE9qFzYpct9pbq22V6SRBZbMVoXbjS4CWBV5r8C8130_assertion
a
np:Assertion
.
dgn-np:NP283992.RAn-MZE9qFzYpct9pbq22V6SRBZbMVoXbjS4CWBV5r8C8130_provenance
a
np:Provenance
.
dgn-np:NP283992.RAn-MZE9qFzYpct9pbq22V6SRBZbMVoXbjS4CWBV5r8C8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP283992.RAn-MZE9qFzYpct9pbq22V6SRBZbMVoXbjS4CWBV5r8C8130_assertion
{
miriam-gene:4233
a
ncit:C16612
.
lld:C0007134
a
ncit:C7057
.
dgn-gda:DGN44abfe3b78e8e3ef28c4feedef81ea12
sio:SIO_000628
miriam-gene:4233
,
lld:C0007134
;
a
sio:SIO_001121
.
}
dgn-np:NP283992.RAn-MZE9qFzYpct9pbq22V6SRBZbMVoXbjS4CWBV5r8C8130_provenance
{
dgn-np:NP283992.RAn-MZE9qFzYpct9pbq22V6SRBZbMVoXbjS4CWBV5r8C8130_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-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:NP283992.RAn-MZE9qFzYpct9pbq22V6SRBZbMVoXbjS4CWBV5r8C8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:54+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" .
}