@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP350839.RAKm3u2Jb2XjxAmEHeyiSZHKaf7wtrDNAmF-ezRO934us
> .
@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:NP350839.RAKm3u2Jb2XjxAmEHeyiSZHKaf7wtrDNAmF-ezRO934us130_head
{
this:
np:hasAssertion
dgn-np:NP350839.RAKm3u2Jb2XjxAmEHeyiSZHKaf7wtrDNAmF-ezRO934us130_assertion
;
np:hasProvenance
dgn-np:NP350839.RAKm3u2Jb2XjxAmEHeyiSZHKaf7wtrDNAmF-ezRO934us130_provenance
;
np:hasPublicationInfo
dgn-np:NP350839.RAKm3u2Jb2XjxAmEHeyiSZHKaf7wtrDNAmF-ezRO934us130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP350839.RAKm3u2Jb2XjxAmEHeyiSZHKaf7wtrDNAmF-ezRO934us130_assertion
a
np:Assertion
.
dgn-np:NP350839.RAKm3u2Jb2XjxAmEHeyiSZHKaf7wtrDNAmF-ezRO934us130_provenance
a
np:Provenance
.
dgn-np:NP350839.RAKm3u2Jb2XjxAmEHeyiSZHKaf7wtrDNAmF-ezRO934us130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP350839.RAKm3u2Jb2XjxAmEHeyiSZHKaf7wtrDNAmF-ezRO934us130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0029463
a
ncit:C7057
.
dgn-gda:DGN0d7de05d6a2d547dcc5b7f78f0b481ea
sio:SIO_000628
miriam-gene:1956
,
lld:C0029463
;
a
sio:SIO_001121
.
}
dgn-np:NP350839.RAKm3u2Jb2XjxAmEHeyiSZHKaf7wtrDNAmF-ezRO934us130_provenance
{
dgn-np:NP350839.RAKm3u2Jb2XjxAmEHeyiSZHKaf7wtrDNAmF-ezRO934us130_assertion
dcterms:description
"[While we were able to show that high frequency of EGFR expression in osteosarcomas is associated with predominantly short alleles of EGFR-CA SSR I, persisting shortcomings in the correspondence with clinical data point toward the existence of additional, putatively more important transcription control mechanisms for EGFR in osteosarcomas which might account for the good prognostic value of EGFR expression.]. 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:18464244
;
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:NP350839.RAKm3u2Jb2XjxAmEHeyiSZHKaf7wtrDNAmF-ezRO934us130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:26+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" .
}