@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP198544.RA6XvSQHngRcG21UXU0Tw0l8gSkxlYwXjIIce-N4GPx14
> .
@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:NP198544.RA6XvSQHngRcG21UXU0Tw0l8gSkxlYwXjIIce-N4GPx14130_head
{
this:
np:hasAssertion
dgn-np:NP198544.RA6XvSQHngRcG21UXU0Tw0l8gSkxlYwXjIIce-N4GPx14130_assertion
;
np:hasProvenance
dgn-np:NP198544.RA6XvSQHngRcG21UXU0Tw0l8gSkxlYwXjIIce-N4GPx14130_provenance
;
np:hasPublicationInfo
dgn-np:NP198544.RA6XvSQHngRcG21UXU0Tw0l8gSkxlYwXjIIce-N4GPx14130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP198544.RA6XvSQHngRcG21UXU0Tw0l8gSkxlYwXjIIce-N4GPx14130_assertion
a
np:Assertion
.
dgn-np:NP198544.RA6XvSQHngRcG21UXU0Tw0l8gSkxlYwXjIIce-N4GPx14130_provenance
a
np:Provenance
.
dgn-np:NP198544.RA6XvSQHngRcG21UXU0Tw0l8gSkxlYwXjIIce-N4GPx14130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP198544.RA6XvSQHngRcG21UXU0Tw0l8gSkxlYwXjIIce-N4GPx14130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0686619
a
ncit:C7057
.
dgn-gda:DGN30373871c33bf5ec4fadd4be89bc950a
sio:SIO_000628
miriam-gene:7157
,
lld:C0686619
;
a
sio:SIO_001121
.
}
dgn-np:NP198544.RA6XvSQHngRcG21UXU0Tw0l8gSkxlYwXjIIce-N4GPx14130_provenance
{
dgn-np:NP198544.RA6XvSQHngRcG21UXU0Tw0l8gSkxlYwXjIIce-N4GPx14130_assertion
dcterms:description
"[The only correlation between these genetic alterations and clinicopathologic characteristics was that mutations of the p53 gene were detected more frequently in oral SCCs with lymph node metastasis than in those without it (P < 0.05).]. 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:8887073
;
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:NP198544.RA6XvSQHngRcG21UXU0Tw0l8gSkxlYwXjIIce-N4GPx14130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:49+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" .
}