@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP695771.RA8Haj6NfC6KpZL3_KkUE4kn7RbgLb6R7qNWOECE9oF1w
> .
@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:NP695771.RA8Haj6NfC6KpZL3_KkUE4kn7RbgLb6R7qNWOECE9oF1w130_head
{
this:
np:hasAssertion
dgn-np:NP695771.RA8Haj6NfC6KpZL3_KkUE4kn7RbgLb6R7qNWOECE9oF1w130_assertion
;
np:hasProvenance
dgn-np:NP695771.RA8Haj6NfC6KpZL3_KkUE4kn7RbgLb6R7qNWOECE9oF1w130_provenance
;
np:hasPublicationInfo
dgn-np:NP695771.RA8Haj6NfC6KpZL3_KkUE4kn7RbgLb6R7qNWOECE9oF1w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP695771.RA8Haj6NfC6KpZL3_KkUE4kn7RbgLb6R7qNWOECE9oF1w130_assertion
a
np:Assertion
.
dgn-np:NP695771.RA8Haj6NfC6KpZL3_KkUE4kn7RbgLb6R7qNWOECE9oF1w130_provenance
a
np:Provenance
.
dgn-np:NP695771.RA8Haj6NfC6KpZL3_KkUE4kn7RbgLb6R7qNWOECE9oF1w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP695771.RA8Haj6NfC6KpZL3_KkUE4kn7RbgLb6R7qNWOECE9oF1w130_assertion
{
miriam-gene:5781
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGNf12197302ac6f5ca1094be4d08cbe69d
sio:SIO_000628
miriam-gene:5781
,
lld:C0007137
;
a
sio:SIO_001121
.
}
dgn-np:NP695771.RA8Haj6NfC6KpZL3_KkUE4kn7RbgLb6R7qNWOECE9oF1w130_provenance
{
dgn-np:NP695771.RA8Haj6NfC6KpZL3_KkUE4kn7RbgLb6R7qNWOECE9oF1w130_assertion
dcterms:description
"[Several novel genes involving the p53 pathway, anti-apoptotic pathways, signal transduction, structural loss and DNA replication, including BCL2A1, MUC4, PTPN11 (SHP2) and FGF9, are upregulated in SCC and could warrant further study regarding their role in disease pathogenesis.]. 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:16700662
;
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:NP695771.RA8Haj6NfC6KpZL3_KkUE4kn7RbgLb6R7qNWOECE9oF1w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:03+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" .
}