@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP329123.RAjBn6OwHhrBNdkqiFO2rkr-HEUsQceeZAqgLAZmnVvts
> .
@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:NP329123.RAjBn6OwHhrBNdkqiFO2rkr-HEUsQceeZAqgLAZmnVvts130_head
{
this:
np:hasAssertion
dgn-np:NP329123.RAjBn6OwHhrBNdkqiFO2rkr-HEUsQceeZAqgLAZmnVvts130_assertion
;
np:hasProvenance
dgn-np:NP329123.RAjBn6OwHhrBNdkqiFO2rkr-HEUsQceeZAqgLAZmnVvts130_provenance
;
np:hasPublicationInfo
dgn-np:NP329123.RAjBn6OwHhrBNdkqiFO2rkr-HEUsQceeZAqgLAZmnVvts130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP329123.RAjBn6OwHhrBNdkqiFO2rkr-HEUsQceeZAqgLAZmnVvts130_assertion
a
np:Assertion
.
dgn-np:NP329123.RAjBn6OwHhrBNdkqiFO2rkr-HEUsQceeZAqgLAZmnVvts130_provenance
a
np:Provenance
.
dgn-np:NP329123.RAjBn6OwHhrBNdkqiFO2rkr-HEUsQceeZAqgLAZmnVvts130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP329123.RAjBn6OwHhrBNdkqiFO2rkr-HEUsQceeZAqgLAZmnVvts130_assertion
{
miriam-gene:2189
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGNe09758bfa3d8fad1eb8e4cd6e162ea01
sio:SIO_000628
miriam-gene:2189
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP329123.RAjBn6OwHhrBNdkqiFO2rkr-HEUsQceeZAqgLAZmnVvts130_provenance
{
dgn-np:NP329123.RAjBn6OwHhrBNdkqiFO2rkr-HEUsQceeZAqgLAZmnVvts130_assertion
dcterms:description
"[While FANCG mutation carrier status does not predispose to sporadic AML, the identification of unrecognised FA patients implies that FA presenting with primary AML in childhood is more common than suspected.]. 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:16643430
;
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:NP329123.RAjBn6OwHhrBNdkqiFO2rkr-HEUsQceeZAqgLAZmnVvts130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:14+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" .
}