@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP623898.RAG1bz_rkNCl9ZihjySObv261eUAPDkL8l42mz1uBz16g
> .
@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:NP623898.RAG1bz_rkNCl9ZihjySObv261eUAPDkL8l42mz1uBz16g130_head
{
this:
np:hasAssertion
dgn-np:NP623898.RAG1bz_rkNCl9ZihjySObv261eUAPDkL8l42mz1uBz16g130_assertion
;
np:hasProvenance
dgn-np:NP623898.RAG1bz_rkNCl9ZihjySObv261eUAPDkL8l42mz1uBz16g130_provenance
;
np:hasPublicationInfo
dgn-np:NP623898.RAG1bz_rkNCl9ZihjySObv261eUAPDkL8l42mz1uBz16g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP623898.RAG1bz_rkNCl9ZihjySObv261eUAPDkL8l42mz1uBz16g130_assertion
a
np:Assertion
.
dgn-np:NP623898.RAG1bz_rkNCl9ZihjySObv261eUAPDkL8l42mz1uBz16g130_provenance
a
np:Provenance
.
dgn-np:NP623898.RAG1bz_rkNCl9ZihjySObv261eUAPDkL8l42mz1uBz16g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP623898.RAG1bz_rkNCl9ZihjySObv261eUAPDkL8l42mz1uBz16g130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0751396
a
ncit:C7057
.
dgn-gda:DGN76fa31fb129de9496a31a2e462ad6a84
sio:SIO_000628
miriam-gene:1956
,
lld:C0751396
;
a
sio:SIO_001121
.
}
dgn-np:NP623898.RAG1bz_rkNCl9ZihjySObv261eUAPDkL8l42mz1uBz16g130_provenance
{
dgn-np:NP623898.RAG1bz_rkNCl9ZihjySObv261eUAPDkL8l42mz1uBz16g130_assertion
dcterms:description
"[LOH on 1p and 19q were associated with oligodendrogliomas, LOH on 10q was related to EGFR amplification, and LOH on 1p and 19q was mutually exclusive with EGFR amplification and LOH on 10q.]. 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:16986124
;
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:NP623898.RAG1bz_rkNCl9ZihjySObv261eUAPDkL8l42mz1uBz16g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:16+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" .
}