@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP268164.RANFxQUke-b_nak0rVd2rvI-rfabatq-M2h8na5l-wOrA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP268164.RANFxQUke-b_nak0rVd2rvI-rfabatq-M2h8na5l-wOrA130_head
{
this:
np:hasAssertion
dgn-np:NP268164.RANFxQUke-b_nak0rVd2rvI-rfabatq-M2h8na5l-wOrA130_assertion
;
np:hasProvenance
dgn-np:NP268164.RANFxQUke-b_nak0rVd2rvI-rfabatq-M2h8na5l-wOrA130_provenance
;
np:hasPublicationInfo
dgn-np:NP268164.RANFxQUke-b_nak0rVd2rvI-rfabatq-M2h8na5l-wOrA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP268164.RANFxQUke-b_nak0rVd2rvI-rfabatq-M2h8na5l-wOrA130_assertion
a
np:Assertion
.
dgn-np:NP268164.RANFxQUke-b_nak0rVd2rvI-rfabatq-M2h8na5l-wOrA130_provenance
a
np:Provenance
.
dgn-np:NP268164.RANFxQUke-b_nak0rVd2rvI-rfabatq-M2h8na5l-wOrA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP268164.RANFxQUke-b_nak0rVd2rvI-rfabatq-M2h8na5l-wOrA130_assertion
{
miriam-gene:641
a
ncit:C16612
.
lld:C1306459
a
ncit:C7057
.
dgn-gda:DGN78eda07d8fef8b272dc49c8979c59362
sio:SIO_000628
miriam-gene:641
,
lld:C1306459
;
a
sio:SIO_001121
.
}
dgn-np:NP268164.RANFxQUke-b_nak0rVd2rvI-rfabatq-M2h8na5l-wOrA130_provenance
{
dgn-np:NP268164.RANFxQUke-b_nak0rVd2rvI-rfabatq-M2h8na5l-wOrA130_assertion
dcterms:description
"[Mutations of the human RecQ helicase genes WRN and BLM lead to rare autosomal recessive disorders, Werner and Bloom syndromes, which are associated with premature aging and cancer predisposition, including breast cancer.]. 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:19205873
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP268164.RANFxQUke-b_nak0rVd2rvI-rfabatq-M2h8na5l-wOrA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:12+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}