@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP806171.RAycVtLXDEEu9ZpieCb505OLNZf4X60BdjwqXCUBtw3cE
> .
@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:NP806171.RAycVtLXDEEu9ZpieCb505OLNZf4X60BdjwqXCUBtw3cE130_head
{
this:
np:hasAssertion
dgn-np:NP806171.RAycVtLXDEEu9ZpieCb505OLNZf4X60BdjwqXCUBtw3cE130_assertion
;
np:hasProvenance
dgn-np:NP806171.RAycVtLXDEEu9ZpieCb505OLNZf4X60BdjwqXCUBtw3cE130_provenance
;
np:hasPublicationInfo
dgn-np:NP806171.RAycVtLXDEEu9ZpieCb505OLNZf4X60BdjwqXCUBtw3cE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP806171.RAycVtLXDEEu9ZpieCb505OLNZf4X60BdjwqXCUBtw3cE130_assertion
a
np:Assertion
.
dgn-np:NP806171.RAycVtLXDEEu9ZpieCb505OLNZf4X60BdjwqXCUBtw3cE130_provenance
a
np:Provenance
.
dgn-np:NP806171.RAycVtLXDEEu9ZpieCb505OLNZf4X60BdjwqXCUBtw3cE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP806171.RAycVtLXDEEu9ZpieCb505OLNZf4X60BdjwqXCUBtw3cE130_assertion
{
miriam-gene:1956
a
ncit:C16612
.
lld:C0521158
a
ncit:C7057
.
dgn-gda:DGN0cf6ed629901fc020a55fdad0257b4d7
sio:SIO_000628
miriam-gene:1956
,
lld:C0521158
;
a
sio:SIO_001121
.
}
dgn-np:NP806171.RAycVtLXDEEu9ZpieCb505OLNZf4X60BdjwqXCUBtw3cE130_provenance
{
dgn-np:NP806171.RAycVtLXDEEu9ZpieCb505OLNZf4X60BdjwqXCUBtw3cE130_assertion
dcterms:description
"[Molecular analysis of tumor DNA from the second recurrent tumor demonstrated the presence of the TP53 mutation, which previously had been observed in the first recurrent tumor, but again no evidence of EGFR amplification.]. 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:11453385
;
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:NP806171.RAycVtLXDEEu9ZpieCb505OLNZf4X60BdjwqXCUBtw3cE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:14+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" .
}