@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP590042.RAIOv4nbz4ng0YLxuXK6fDPwarh9txBp_8WysKLtWPMZs
> .
@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:NP590042.RAIOv4nbz4ng0YLxuXK6fDPwarh9txBp_8WysKLtWPMZs130_head
{
this:
np:hasAssertion
dgn-np:NP590042.RAIOv4nbz4ng0YLxuXK6fDPwarh9txBp_8WysKLtWPMZs130_assertion
;
np:hasProvenance
dgn-np:NP590042.RAIOv4nbz4ng0YLxuXK6fDPwarh9txBp_8WysKLtWPMZs130_provenance
;
np:hasPublicationInfo
dgn-np:NP590042.RAIOv4nbz4ng0YLxuXK6fDPwarh9txBp_8WysKLtWPMZs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP590042.RAIOv4nbz4ng0YLxuXK6fDPwarh9txBp_8WysKLtWPMZs130_assertion
a
np:Assertion
.
dgn-np:NP590042.RAIOv4nbz4ng0YLxuXK6fDPwarh9txBp_8WysKLtWPMZs130_provenance
a
np:Provenance
.
dgn-np:NP590042.RAIOv4nbz4ng0YLxuXK6fDPwarh9txBp_8WysKLtWPMZs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP590042.RAIOv4nbz4ng0YLxuXK6fDPwarh9txBp_8WysKLtWPMZs130_assertion
{
miriam-gene:571
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGNe7024efa4a92ed8936506569215d4999
sio:SIO_000628
miriam-gene:571
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP590042.RAIOv4nbz4ng0YLxuXK6fDPwarh9txBp_8WysKLtWPMZs130_provenance
{
dgn-np:NP590042.RAIOv4nbz4ng0YLxuXK6fDPwarh9txBp_8WysKLtWPMZs130_assertion
dcterms:description
"[It is clear that FANCJ, also known as BACH1 or BRIP1, is an essential tumor suppressor gene based on the identification of clinically relevant mutations not only in breast cancer, but also the childhood cancer syndrome, Fanconi anemia.]. 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:21345144
;
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:NP590042.RAIOv4nbz4ng0YLxuXK6fDPwarh9txBp_8WysKLtWPMZs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:55+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" .
}