@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP870920.RAtXlFX8e4OhQYWC4bNmUhIJC68LhnWP1YHMQY-K_Imvk
> .
@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:NP870920.RAtXlFX8e4OhQYWC4bNmUhIJC68LhnWP1YHMQY-K_Imvk130_head
{
this:
np:hasAssertion
dgn-np:NP870920.RAtXlFX8e4OhQYWC4bNmUhIJC68LhnWP1YHMQY-K_Imvk130_assertion
;
np:hasProvenance
dgn-np:NP870920.RAtXlFX8e4OhQYWC4bNmUhIJC68LhnWP1YHMQY-K_Imvk130_provenance
;
np:hasPublicationInfo
dgn-np:NP870920.RAtXlFX8e4OhQYWC4bNmUhIJC68LhnWP1YHMQY-K_Imvk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP870920.RAtXlFX8e4OhQYWC4bNmUhIJC68LhnWP1YHMQY-K_Imvk130_assertion
a
np:Assertion
.
dgn-np:NP870920.RAtXlFX8e4OhQYWC4bNmUhIJC68LhnWP1YHMQY-K_Imvk130_provenance
a
np:Provenance
.
dgn-np:NP870920.RAtXlFX8e4OhQYWC4bNmUhIJC68LhnWP1YHMQY-K_Imvk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP870920.RAtXlFX8e4OhQYWC4bNmUhIJC68LhnWP1YHMQY-K_Imvk130_assertion
{
miriam-gene:6223
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN856ce1a0e8f923de9466d1bc4fc8af4b
sio:SIO_000628
miriam-gene:6223
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP870920.RAtXlFX8e4OhQYWC4bNmUhIJC68LhnWP1YHMQY-K_Imvk130_provenance
{
dgn-np:NP870920.RAtXlFX8e4OhQYWC4bNmUhIJC68LhnWP1YHMQY-K_Imvk130_assertion
dcterms:description
"[Using this database, important epidemiologic, clinical, and laboratory observations have been made with regard to the clinical presentation, the inheritance of DBA, the genetics of congenital malformations, the therapeutic outcome, including the efficacy of hematopoietic stem cell transplantation, and the recognition of DBA as a cancer predisposition syndrome.]. 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:11563775
;
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:NP870920.RAtXlFX8e4OhQYWC4bNmUhIJC68LhnWP1YHMQY-K_Imvk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:52+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" .
}