@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP776433.RAbFoutepM-Ea15AsSN9W7RqxWvH2de50kZJm2y8TXfTw
> .
@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:NP776433.RAbFoutepM-Ea15AsSN9W7RqxWvH2de50kZJm2y8TXfTw130_head
{
this:
np:hasAssertion
dgn-np:NP776433.RAbFoutepM-Ea15AsSN9W7RqxWvH2de50kZJm2y8TXfTw130_assertion
;
np:hasProvenance
dgn-np:NP776433.RAbFoutepM-Ea15AsSN9W7RqxWvH2de50kZJm2y8TXfTw130_provenance
;
np:hasPublicationInfo
dgn-np:NP776433.RAbFoutepM-Ea15AsSN9W7RqxWvH2de50kZJm2y8TXfTw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP776433.RAbFoutepM-Ea15AsSN9W7RqxWvH2de50kZJm2y8TXfTw130_assertion
a
np:Assertion
.
dgn-np:NP776433.RAbFoutepM-Ea15AsSN9W7RqxWvH2de50kZJm2y8TXfTw130_provenance
a
np:Provenance
.
dgn-np:NP776433.RAbFoutepM-Ea15AsSN9W7RqxWvH2de50kZJm2y8TXfTw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP776433.RAbFoutepM-Ea15AsSN9W7RqxWvH2de50kZJm2y8TXfTw130_assertion
{
miriam-gene:3014
a
ncit:C16612
.
lld:C0005859
a
ncit:C7057
.
dgn-gda:DGN08d92072541467fa97f96593c5f937f0
sio:SIO_000628
miriam-gene:3014
,
lld:C0005859
;
a
sio:SIO_001121
.
}
dgn-np:NP776433.RAbFoutepM-Ea15AsSN9W7RqxWvH2de50kZJm2y8TXfTw130_provenance
{
dgn-np:NP776433.RAbFoutepM-Ea15AsSN9W7RqxWvH2de50kZJm2y8TXfTw130_assertion
dcterms:description
"[These abnormalities are not associated with a failure of the BLM-T99A/T122A protein to localize to replication foci or to colocalize either with ATR itself or with other proteins that are required for response to DNA damage, such as phosphorylated histone H2AX and RAD51.]. 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:14729972
;
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:NP776433.RAbFoutepM-Ea15AsSN9W7RqxWvH2de50kZJm2y8TXfTw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:50+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" .
}