@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP828393.RAl_WUCnmLzJ6ycUzXpY_u0H-CmTtoOiYFQddJcEbcTX8
> .
@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:NP828393.RAl_WUCnmLzJ6ycUzXpY_u0H-CmTtoOiYFQddJcEbcTX8130_head
{
this:
np:hasAssertion
dgn-np:NP828393.RAl_WUCnmLzJ6ycUzXpY_u0H-CmTtoOiYFQddJcEbcTX8130_assertion
;
np:hasProvenance
dgn-np:NP828393.RAl_WUCnmLzJ6ycUzXpY_u0H-CmTtoOiYFQddJcEbcTX8130_provenance
;
np:hasPublicationInfo
dgn-np:NP828393.RAl_WUCnmLzJ6ycUzXpY_u0H-CmTtoOiYFQddJcEbcTX8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP828393.RAl_WUCnmLzJ6ycUzXpY_u0H-CmTtoOiYFQddJcEbcTX8130_assertion
a
np:Assertion
.
dgn-np:NP828393.RAl_WUCnmLzJ6ycUzXpY_u0H-CmTtoOiYFQddJcEbcTX8130_provenance
a
np:Provenance
.
dgn-np:NP828393.RAl_WUCnmLzJ6ycUzXpY_u0H-CmTtoOiYFQddJcEbcTX8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP828393.RAl_WUCnmLzJ6ycUzXpY_u0H-CmTtoOiYFQddJcEbcTX8130_assertion
{
miriam-gene:8061
a
ncit:C16612
.
lld:C1458155
a
ncit:C7057
.
dgn-gda:DGN15d8a19a6227c3cb948826c83a84651d
sio:SIO_000628
miriam-gene:8061
,
lld:C1458155
;
a
sio:SIO_001121
.
}
dgn-np:NP828393.RAl_WUCnmLzJ6ycUzXpY_u0H-CmTtoOiYFQddJcEbcTX8130_provenance
{
dgn-np:NP828393.RAl_WUCnmLzJ6ycUzXpY_u0H-CmTtoOiYFQddJcEbcTX8130_assertion
dcterms:description
"[The FHIT gene is located at the FRA 3B fragile site at chromosome 3p 14.2, and alterations in the FHIT gene and Fhit protein have been found associated with genome instability, particularly in BRCA 2 mutated breast tumours.]. 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:11562178
;
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:NP828393.RAl_WUCnmLzJ6ycUzXpY_u0H-CmTtoOiYFQddJcEbcTX8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:27+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" .
}