@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo
> .
@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:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_head
{
this:
np:hasAssertion
dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_assertion
;
np:hasProvenance
dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_provenance
;
np:hasPublicationInfo
dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_assertion
a
np:Assertion
.
dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_provenance
a
np:Provenance
.
dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_assertion
{
miriam-gene:2274
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGNd51db879fbc6b182364bcee5290e3df0
sio:SIO_000628
miriam-gene:2274
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_provenance
{
dgn-np:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_assertion
dcterms:description
"[Since transcription factors control all fundamental developmental and homeostatic processes, transcriptional cofactors like FHL2 are likely to contribute to human carcinogenesis and are of clinical importance in various forms of cancer.]. 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:17352216
;
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:NP455806.RAw7EaXhyCmSTItQgNVXGAF6_SL9SwqUK77U9GOBokmTo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:31+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" .
}