@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP175094.RAOPQbvnRcJ-NxYnwlybfBOY-2Y0ZhuWZl5h61FS5rqnI
> .
@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:NP175094.RAOPQbvnRcJ-NxYnwlybfBOY-2Y0ZhuWZl5h61FS5rqnI130_head
{
this:
np:hasAssertion
dgn-np:NP175094.RAOPQbvnRcJ-NxYnwlybfBOY-2Y0ZhuWZl5h61FS5rqnI130_assertion
;
np:hasProvenance
dgn-np:NP175094.RAOPQbvnRcJ-NxYnwlybfBOY-2Y0ZhuWZl5h61FS5rqnI130_provenance
;
np:hasPublicationInfo
dgn-np:NP175094.RAOPQbvnRcJ-NxYnwlybfBOY-2Y0ZhuWZl5h61FS5rqnI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP175094.RAOPQbvnRcJ-NxYnwlybfBOY-2Y0ZhuWZl5h61FS5rqnI130_assertion
a
np:Assertion
.
dgn-np:NP175094.RAOPQbvnRcJ-NxYnwlybfBOY-2Y0ZhuWZl5h61FS5rqnI130_provenance
a
np:Provenance
.
dgn-np:NP175094.RAOPQbvnRcJ-NxYnwlybfBOY-2Y0ZhuWZl5h61FS5rqnI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP175094.RAOPQbvnRcJ-NxYnwlybfBOY-2Y0ZhuWZl5h61FS5rqnI130_assertion
{
miriam-gene:7486
a
ncit:C16612
.
lld:C0231341
a
ncit:C7057
.
dgn-gda:DGN9f0c2aed2452134ca41a0a47607483ad
sio:SIO_000628
miriam-gene:7486
,
lld:C0231341
;
a
sio:SIO_001121
.
}
dgn-np:NP175094.RAOPQbvnRcJ-NxYnwlybfBOY-2Y0ZhuWZl5h61FS5rqnI130_provenance
{
dgn-np:NP175094.RAOPQbvnRcJ-NxYnwlybfBOY-2Y0ZhuWZl5h61FS5rqnI130_assertion
dcterms:description
"[Mutations in three of the five known family members in humans, BLM, WRN and RECQL4, give rise to disorders that are characterized by predisposition to cancer and premature aging, emphasizing the importance of studying the RecQ proteins and their cellular activities.]. 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:17364146
;
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:NP175094.RAOPQbvnRcJ-NxYnwlybfBOY-2Y0ZhuWZl5h61FS5rqnI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:34+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" .
}