@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP776585.RAfXSEIyg1eNrHvqwB4-IwGf6o0bCZOiK2ul38QqCaKy4
> .
@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:NP776585.RAfXSEIyg1eNrHvqwB4-IwGf6o0bCZOiK2ul38QqCaKy4130_head
{
this:
np:hasAssertion
dgn-np:NP776585.RAfXSEIyg1eNrHvqwB4-IwGf6o0bCZOiK2ul38QqCaKy4130_assertion
;
np:hasProvenance
dgn-np:NP776585.RAfXSEIyg1eNrHvqwB4-IwGf6o0bCZOiK2ul38QqCaKy4130_provenance
;
np:hasPublicationInfo
dgn-np:NP776585.RAfXSEIyg1eNrHvqwB4-IwGf6o0bCZOiK2ul38QqCaKy4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP776585.RAfXSEIyg1eNrHvqwB4-IwGf6o0bCZOiK2ul38QqCaKy4130_assertion
a
np:Assertion
.
dgn-np:NP776585.RAfXSEIyg1eNrHvqwB4-IwGf6o0bCZOiK2ul38QqCaKy4130_provenance
a
np:Provenance
.
dgn-np:NP776585.RAfXSEIyg1eNrHvqwB4-IwGf6o0bCZOiK2ul38QqCaKy4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP776585.RAfXSEIyg1eNrHvqwB4-IwGf6o0bCZOiK2ul38QqCaKy4130_assertion
{
miriam-gene:3845
a
ncit:C16612
.
lld:C0206698
a
ncit:C7057
.
dgn-gda:DGN84cb016b871bcae2618f8149e0e3bb7d
sio:SIO_000628
miriam-gene:3845
,
lld:C0206698
;
a
sio:SIO_001121
.
}
dgn-np:NP776585.RAfXSEIyg1eNrHvqwB4-IwGf6o0bCZOiK2ul38QqCaKy4130_provenance
{
dgn-np:NP776585.RAfXSEIyg1eNrHvqwB4-IwGf6o0bCZOiK2ul38QqCaKy4130_assertion
dcterms:description
"[β-catenin and P53 mutations represent the two main genetic alterations described in HCC, and P53 and KRAS mutations in CC, but rare genetic alterations could be particularly valuable if they constitute drug-able targets (such as PIK3CA or EGFR mutations).]. 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:21538283
;
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:NP776585.RAfXSEIyg1eNrHvqwB4-IwGf6o0bCZOiK2ul38QqCaKy4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:50+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" .
}