@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP360812.RA3AKoXfxdk_AIB7cjmrX5Dvd2gYQ1vyD0a6SxQMhpGG8
> .
@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:NP360812.RA3AKoXfxdk_AIB7cjmrX5Dvd2gYQ1vyD0a6SxQMhpGG8130_head
{
this:
np:hasAssertion
dgn-np:NP360812.RA3AKoXfxdk_AIB7cjmrX5Dvd2gYQ1vyD0a6SxQMhpGG8130_assertion
;
np:hasProvenance
dgn-np:NP360812.RA3AKoXfxdk_AIB7cjmrX5Dvd2gYQ1vyD0a6SxQMhpGG8130_provenance
;
np:hasPublicationInfo
dgn-np:NP360812.RA3AKoXfxdk_AIB7cjmrX5Dvd2gYQ1vyD0a6SxQMhpGG8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP360812.RA3AKoXfxdk_AIB7cjmrX5Dvd2gYQ1vyD0a6SxQMhpGG8130_assertion
a
np:Assertion
.
dgn-np:NP360812.RA3AKoXfxdk_AIB7cjmrX5Dvd2gYQ1vyD0a6SxQMhpGG8130_provenance
a
np:Provenance
.
dgn-np:NP360812.RA3AKoXfxdk_AIB7cjmrX5Dvd2gYQ1vyD0a6SxQMhpGG8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP360812.RA3AKoXfxdk_AIB7cjmrX5Dvd2gYQ1vyD0a6SxQMhpGG8130_assertion
{
miriam-gene:3371
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNb6643b7ffd5e55a6fb31402d4279afcb
sio:SIO_000628
miriam-gene:3371
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP360812.RA3AKoXfxdk_AIB7cjmrX5Dvd2gYQ1vyD0a6SxQMhpGG8130_provenance
{
dgn-np:NP360812.RA3AKoXfxdk_AIB7cjmrX5Dvd2gYQ1vyD0a6SxQMhpGG8130_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:NP360812.RA3AKoXfxdk_AIB7cjmrX5Dvd2gYQ1vyD0a6SxQMhpGG8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:31+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" .
}