@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP760714.RAUVDuAYhnEVwBVJAnNH7XZrqp3A_WStKtR_IqK11FE60
> .
@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:NP760714.RAUVDuAYhnEVwBVJAnNH7XZrqp3A_WStKtR_IqK11FE60130_head
{
this:
np:hasAssertion
dgn-np:NP760714.RAUVDuAYhnEVwBVJAnNH7XZrqp3A_WStKtR_IqK11FE60130_assertion
;
np:hasProvenance
dgn-np:NP760714.RAUVDuAYhnEVwBVJAnNH7XZrqp3A_WStKtR_IqK11FE60130_provenance
;
np:hasPublicationInfo
dgn-np:NP760714.RAUVDuAYhnEVwBVJAnNH7XZrqp3A_WStKtR_IqK11FE60130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP760714.RAUVDuAYhnEVwBVJAnNH7XZrqp3A_WStKtR_IqK11FE60130_assertion
a
np:Assertion
.
dgn-np:NP760714.RAUVDuAYhnEVwBVJAnNH7XZrqp3A_WStKtR_IqK11FE60130_provenance
a
np:Provenance
.
dgn-np:NP760714.RAUVDuAYhnEVwBVJAnNH7XZrqp3A_WStKtR_IqK11FE60130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP760714.RAUVDuAYhnEVwBVJAnNH7XZrqp3A_WStKtR_IqK11FE60130_assertion
{
miriam-gene:57045
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGNa33e3a0b6833e5209868a82e5ac1075a
sio:SIO_000628
miriam-gene:57045
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP760714.RAUVDuAYhnEVwBVJAnNH7XZrqp3A_WStKtR_IqK11FE60130_provenance
{
dgn-np:NP760714.RAUVDuAYhnEVwBVJAnNH7XZrqp3A_WStKtR_IqK11FE60130_assertion
dcterms:description
"[Loss of heterozygosity (LOH) has been frequently detected at chromosome 7q31 region in human head and neck squamous cell carcinomas (HNSCC) and many other cancers, suggesting the existence of tumor suppressor genes (TSG).]. 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:12080476
;
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:NP760714.RAUVDuAYhnEVwBVJAnNH7XZrqp3A_WStKtR_IqK11FE60130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:40+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" .
}