@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP701226.RAk7TWyVb5TY9nbfpbnnGICOd-Vo1HHu7VarWZAUFSuuM
> .
@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:NP701226.RAk7TWyVb5TY9nbfpbnnGICOd-Vo1HHu7VarWZAUFSuuM130_head
{
this:
np:hasAssertion
dgn-np:NP701226.RAk7TWyVb5TY9nbfpbnnGICOd-Vo1HHu7VarWZAUFSuuM130_assertion
;
np:hasProvenance
dgn-np:NP701226.RAk7TWyVb5TY9nbfpbnnGICOd-Vo1HHu7VarWZAUFSuuM130_provenance
;
np:hasPublicationInfo
dgn-np:NP701226.RAk7TWyVb5TY9nbfpbnnGICOd-Vo1HHu7VarWZAUFSuuM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP701226.RAk7TWyVb5TY9nbfpbnnGICOd-Vo1HHu7VarWZAUFSuuM130_assertion
a
np:Assertion
.
dgn-np:NP701226.RAk7TWyVb5TY9nbfpbnnGICOd-Vo1HHu7VarWZAUFSuuM130_provenance
a
np:Provenance
.
dgn-np:NP701226.RAk7TWyVb5TY9nbfpbnnGICOd-Vo1HHu7VarWZAUFSuuM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP701226.RAk7TWyVb5TY9nbfpbnnGICOd-Vo1HHu7VarWZAUFSuuM130_assertion
{
miriam-gene:1647
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN5dddf3d4f3f190259df16e0042b06f84
sio:SIO_000628
miriam-gene:1647
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP701226.RAk7TWyVb5TY9nbfpbnnGICOd-Vo1HHu7VarWZAUFSuuM130_provenance
{
dgn-np:NP701226.RAk7TWyVb5TY9nbfpbnnGICOd-Vo1HHu7VarWZAUFSuuM130_assertion
dcterms:description
"[The AT gene product would thus appear to be involved upstream of p53, GADD45 and WAF1/CIP1 (p21) in the signalling of the presence of strand breaks produced by ionising radiation, with this defect in response contributing to the high cancer risk and radiosensitivity observed in this disorder.]. 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:7478567
;
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:NP701226.RAk7TWyVb5TY9nbfpbnnGICOd-Vo1HHu7VarWZAUFSuuM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:06+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" .
}