@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc
> .
@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:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_head
{
this:
np:hasAssertion
dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_assertion
;
np:hasProvenance
dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_provenance
;
np:hasPublicationInfo
dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_assertion
a
np:Assertion
.
dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_provenance
a
np:Provenance
.
dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_assertion
{
miriam-gene:545
a
ncit:C16612
.
lld:C0004135
a
ncit:C7057
.
dgn-gda:DGN865f86066f49a7fd229f086cca84132c
sio:SIO_000628
miriam-gene:545
,
lld:C0004135
;
a
sio:SIO_001121
.
}
dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_provenance
{
dgn-np:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_assertion
dcterms:description
"[Based on the homology of the human ATM gene to the TEL1, MEC1 and rad3 genes of yeast, it has now been demonstrated that mutations in ATM lead to defective telomere maintenance in mammalian cells.]. 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:11850786
;
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:NP690044.RA4CjcpUVLR9nNnSt_DsCUinrgZPsLPZLxLBgkP_ECbvc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:59+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" .
}