@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP644067.RAu_RvIZzWwQ2-DWETzV4whX7HsqoTcT5X7PHW-JJTx-I
> .
@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:NP644067.RAu_RvIZzWwQ2-DWETzV4whX7HsqoTcT5X7PHW-JJTx-I130_head
{
this:
np:hasAssertion
dgn-np:NP644067.RAu_RvIZzWwQ2-DWETzV4whX7HsqoTcT5X7PHW-JJTx-I130_assertion
;
np:hasProvenance
dgn-np:NP644067.RAu_RvIZzWwQ2-DWETzV4whX7HsqoTcT5X7PHW-JJTx-I130_provenance
;
np:hasPublicationInfo
dgn-np:NP644067.RAu_RvIZzWwQ2-DWETzV4whX7HsqoTcT5X7PHW-JJTx-I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP644067.RAu_RvIZzWwQ2-DWETzV4whX7HsqoTcT5X7PHW-JJTx-I130_assertion
a
np:Assertion
.
dgn-np:NP644067.RAu_RvIZzWwQ2-DWETzV4whX7HsqoTcT5X7PHW-JJTx-I130_provenance
a
np:Provenance
.
dgn-np:NP644067.RAu_RvIZzWwQ2-DWETzV4whX7HsqoTcT5X7PHW-JJTx-I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP644067.RAu_RvIZzWwQ2-DWETzV4whX7HsqoTcT5X7PHW-JJTx-I130_assertion
{
miriam-gene:3417
a
ncit:C16612
.
lld:C0263214
a
ncit:C7057
.
dgn-gda:DGNd9c6e0c00ff7b7698fd655c5dc925ca0
sio:SIO_000628
miriam-gene:3417
,
lld:C0263214
;
a
sio:SIO_001121
.
}
dgn-np:NP644067.RAu_RvIZzWwQ2-DWETzV4whX7HsqoTcT5X7PHW-JJTx-I130_provenance
{
dgn-np:NP644067.RAu_RvIZzWwQ2-DWETzV4whX7HsqoTcT5X7PHW-JJTx-I130_assertion
dcterms:description
"[By direct genomic DNA sequencing, we analyzed exon 4 of the IDH1 and IDH2 genes that harbored the mutation hot spots codon 132 and 172 of the two genes in glioblastoma, respectively, in 12 thyroid cancer cell lines, 20 FTC, and 18 ATC tumor samples.]. 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:20171178
;
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:NP644067.RAu_RvIZzWwQ2-DWETzV4whX7HsqoTcT5X7PHW-JJTx-I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:28+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" .
}