@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP574421.RASFRbpT9MiwfgaJn0GZiiLTlmiJ0dl0bDquGZfYjRQrU
> .
@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:NP574421.RASFRbpT9MiwfgaJn0GZiiLTlmiJ0dl0bDquGZfYjRQrU130_head
{
this:
np:hasAssertion
dgn-np:NP574421.RASFRbpT9MiwfgaJn0GZiiLTlmiJ0dl0bDquGZfYjRQrU130_assertion
;
np:hasProvenance
dgn-np:NP574421.RASFRbpT9MiwfgaJn0GZiiLTlmiJ0dl0bDquGZfYjRQrU130_provenance
;
np:hasPublicationInfo
dgn-np:NP574421.RASFRbpT9MiwfgaJn0GZiiLTlmiJ0dl0bDquGZfYjRQrU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP574421.RASFRbpT9MiwfgaJn0GZiiLTlmiJ0dl0bDquGZfYjRQrU130_assertion
a
np:Assertion
.
dgn-np:NP574421.RASFRbpT9MiwfgaJn0GZiiLTlmiJ0dl0bDquGZfYjRQrU130_provenance
a
np:Provenance
.
dgn-np:NP574421.RASFRbpT9MiwfgaJn0GZiiLTlmiJ0dl0bDquGZfYjRQrU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP574421.RASFRbpT9MiwfgaJn0GZiiLTlmiJ0dl0bDquGZfYjRQrU130_assertion
{
miriam-gene:5519
a
ncit:C16612
.
lld:C0302592
a
ncit:C7057
.
dgn-gda:DGN4235e5b10e8cd3c9abb293383a050492
sio:SIO_000628
miriam-gene:5519
,
lld:C0302592
;
a
sio:SIO_001121
.
}
dgn-np:NP574421.RASFRbpT9MiwfgaJn0GZiiLTlmiJ0dl0bDquGZfYjRQrU130_provenance
{
dgn-np:NP574421.RASFRbpT9MiwfgaJn0GZiiLTlmiJ0dl0bDquGZfYjRQrU130_assertion
dcterms:description
"[The two genes, PPP2R1B and SDHD, lying in between ATM and CADM1, have low frequency of alterations, and majority of the alterations are in CACX samples, indicating that their alterations might be associated with disease progression.]. 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:21643982
;
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:NP574421.RASFRbpT9MiwfgaJn0GZiiLTlmiJ0dl0bDquGZfYjRQrU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:46+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" .
}