@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes
> .
@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:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_head
{
this:
np:hasAssertion
dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_assertion
;
np:hasProvenance
dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_provenance
;
np:hasPublicationInfo
dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_assertion
a
np:Assertion
.
dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_provenance
a
np:Provenance
.
dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_assertion
{
miriam-gene:5925
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGN633ab2a592d02e3c647c516c600c1a54
sio:SIO_000628
miriam-gene:5925
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_provenance
{
dgn-np:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_assertion
dcterms:description
"[Thus, it seems that the putative TSGs located in the BRCAX and 13q31.1 regions as well as the BRCA2 and RB1 genes may have some cumulative effect in progression and poor prognosis of HNSCC.]. 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:16623759
;
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:NP394817.RAy3_smytX-RIn8vBu1hVbBZ_lMoZJ45bjBPQ7r-tpyes130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:55+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" .
}