@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP583967.RAn7fee6rOT63dEkOErt5yGm-HiQsB5feU9vPB7dnJzCw
> .
@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:NP583967.RAn7fee6rOT63dEkOErt5yGm-HiQsB5feU9vPB7dnJzCw130_head
{
this:
np:hasAssertion
dgn-np:NP583967.RAn7fee6rOT63dEkOErt5yGm-HiQsB5feU9vPB7dnJzCw130_assertion
;
np:hasProvenance
dgn-np:NP583967.RAn7fee6rOT63dEkOErt5yGm-HiQsB5feU9vPB7dnJzCw130_provenance
;
np:hasPublicationInfo
dgn-np:NP583967.RAn7fee6rOT63dEkOErt5yGm-HiQsB5feU9vPB7dnJzCw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP583967.RAn7fee6rOT63dEkOErt5yGm-HiQsB5feU9vPB7dnJzCw130_assertion
a
np:Assertion
.
dgn-np:NP583967.RAn7fee6rOT63dEkOErt5yGm-HiQsB5feU9vPB7dnJzCw130_provenance
a
np:Provenance
.
dgn-np:NP583967.RAn7fee6rOT63dEkOErt5yGm-HiQsB5feU9vPB7dnJzCw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP583967.RAn7fee6rOT63dEkOErt5yGm-HiQsB5feU9vPB7dnJzCw130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0039483
a
ncit:C7057
.
dgn-gda:DGN0605d2c0d7a491b9419300416db6340f
sio:SIO_000628
miriam-gene:7157
,
lld:C0039483
;
a
sio:SIO_001121
.
}
dgn-np:NP583967.RAn7fee6rOT63dEkOErt5yGm-HiQsB5feU9vPB7dnJzCw130_provenance
{
dgn-np:NP583967.RAn7fee6rOT63dEkOErt5yGm-HiQsB5feU9vPB7dnJzCw130_assertion
dcterms:description
"[The accumulated data about the changes of tumor suppressor gene, such as p53 mutation, and ontogeny, such as C-erbB2, especially the similar alterations in GCA and SCC in the same patient, indicated that there might be some similar risk factors, such as nitrosamine, involved in both GCA and SCC in Henan population.]. 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:12800215
;
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:NP583967.RAn7fee6rOT63dEkOErt5yGm-HiQsB5feU9vPB7dnJzCw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:51+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" .
}