@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP277404.RAMK6J1bgS99S3uOOaCRcl16HgQRHLUy4ZSjU7bxZ79mQ
> .
@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:NP277404.RAMK6J1bgS99S3uOOaCRcl16HgQRHLUy4ZSjU7bxZ79mQ130_head
{
this:
np:hasAssertion
dgn-np:NP277404.RAMK6J1bgS99S3uOOaCRcl16HgQRHLUy4ZSjU7bxZ79mQ130_assertion
;
np:hasProvenance
dgn-np:NP277404.RAMK6J1bgS99S3uOOaCRcl16HgQRHLUy4ZSjU7bxZ79mQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP277404.RAMK6J1bgS99S3uOOaCRcl16HgQRHLUy4ZSjU7bxZ79mQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP277404.RAMK6J1bgS99S3uOOaCRcl16HgQRHLUy4ZSjU7bxZ79mQ130_assertion
a
np:Assertion
.
dgn-np:NP277404.RAMK6J1bgS99S3uOOaCRcl16HgQRHLUy4ZSjU7bxZ79mQ130_provenance
a
np:Provenance
.
dgn-np:NP277404.RAMK6J1bgS99S3uOOaCRcl16HgQRHLUy4ZSjU7bxZ79mQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP277404.RAMK6J1bgS99S3uOOaCRcl16HgQRHLUy4ZSjU7bxZ79mQ130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C1368683
a
ncit:C7057
.
dgn-gda:DGN5123b5f748cc855930c86d04af8075f9
sio:SIO_000628
miriam-gene:2272
,
lld:C1368683
;
a
sio:SIO_001121
.
}
dgn-np:NP277404.RAMK6J1bgS99S3uOOaCRcl16HgQRHLUy4ZSjU7bxZ79mQ130_provenance
{
dgn-np:NP277404.RAMK6J1bgS99S3uOOaCRcl16HgQRHLUy4ZSjU7bxZ79mQ130_assertion
dcterms:description
"[The expression of two tumor suppressor genes, fragile histidine triad (FHIT) and WW domain containing oxidoreductase (WWOX), encompassing common chromosome fragile regions, FRA3B at 3p14.2 and FRA16D at 16q23, is altered in many epithelial tumors.]. 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:15044096
;
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:NP277404.RAMK6J1bgS99S3uOOaCRcl16HgQRHLUy4ZSjU7bxZ79mQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:36+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" .
}