@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP601535.RALUThybR1gVvEty8uPTUV37j_RM3rRkL048sxuwNBEnY
> .
@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:NP601535.RALUThybR1gVvEty8uPTUV37j_RM3rRkL048sxuwNBEnY130_head
{
this:
np:hasAssertion
dgn-np:NP601535.RALUThybR1gVvEty8uPTUV37j_RM3rRkL048sxuwNBEnY130_assertion
;
np:hasProvenance
dgn-np:NP601535.RALUThybR1gVvEty8uPTUV37j_RM3rRkL048sxuwNBEnY130_provenance
;
np:hasPublicationInfo
dgn-np:NP601535.RALUThybR1gVvEty8uPTUV37j_RM3rRkL048sxuwNBEnY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP601535.RALUThybR1gVvEty8uPTUV37j_RM3rRkL048sxuwNBEnY130_assertion
a
np:Assertion
.
dgn-np:NP601535.RALUThybR1gVvEty8uPTUV37j_RM3rRkL048sxuwNBEnY130_provenance
a
np:Provenance
.
dgn-np:NP601535.RALUThybR1gVvEty8uPTUV37j_RM3rRkL048sxuwNBEnY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP601535.RALUThybR1gVvEty8uPTUV37j_RM3rRkL048sxuwNBEnY130_assertion
{
miriam-gene:3371
a
ncit:C16612
.
lld:C0086692
a
ncit:C7057
.
dgn-gda:DGN909faf4f92c2213e474601d9a822bd32
sio:SIO_000628
miriam-gene:3371
,
lld:C0086692
;
a
sio:SIO_001121
.
}
dgn-np:NP601535.RALUThybR1gVvEty8uPTUV37j_RM3rRkL048sxuwNBEnY130_provenance
{
dgn-np:NP601535.RALUThybR1gVvEty8uPTUV37j_RM3rRkL048sxuwNBEnY130_assertion
dcterms:description
"[The smallest TN RNA splice variant (284 bp) was found in all tumours examined, while the appearance of larger molecular weight transcripts (approximately 490 and 556 bp), as major forms, was predominantly limited to malignant tumours, with 9/12 malignant tumours showing this pattern compared with 1/6 benign tumours.]. 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:8855965
;
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:NP601535.RALUThybR1gVvEty8uPTUV37j_RM3rRkL048sxuwNBEnY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:01+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" .
}