@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP896993.RAhgPIv7Kn4VngYZvJt-pym3gBf6wrboTMzw3ZVgQVGh4
> .
@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:NP896993.RAhgPIv7Kn4VngYZvJt-pym3gBf6wrboTMzw3ZVgQVGh4130_head
{
this:
np:hasAssertion
dgn-np:NP896993.RAhgPIv7Kn4VngYZvJt-pym3gBf6wrboTMzw3ZVgQVGh4130_assertion
;
np:hasProvenance
dgn-np:NP896993.RAhgPIv7Kn4VngYZvJt-pym3gBf6wrboTMzw3ZVgQVGh4130_provenance
;
np:hasPublicationInfo
dgn-np:NP896993.RAhgPIv7Kn4VngYZvJt-pym3gBf6wrboTMzw3ZVgQVGh4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP896993.RAhgPIv7Kn4VngYZvJt-pym3gBf6wrboTMzw3ZVgQVGh4130_assertion
a
np:Assertion
.
dgn-np:NP896993.RAhgPIv7Kn4VngYZvJt-pym3gBf6wrboTMzw3ZVgQVGh4130_provenance
a
np:Provenance
.
dgn-np:NP896993.RAhgPIv7Kn4VngYZvJt-pym3gBf6wrboTMzw3ZVgQVGh4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP896993.RAhgPIv7Kn4VngYZvJt-pym3gBf6wrboTMzw3ZVgQVGh4130_assertion
{
miriam-gene:1111
a
ncit:C16612
.
lld:C0015625
a
ncit:C7057
.
dgn-gda:DGN30a2bcbc3008fe6eea62e86b864ed0c5
sio:SIO_000628
miriam-gene:1111
,
lld:C0015625
;
a
sio:SIO_001121
.
}
dgn-np:NP896993.RAhgPIv7Kn4VngYZvJt-pym3gBf6wrboTMzw3ZVgQVGh4130_provenance
{
dgn-np:NP896993.RAhgPIv7Kn4VngYZvJt-pym3gBf6wrboTMzw3ZVgQVGh4130_assertion
dcterms:description
"[We show that S1045 is required for FANCM functions including its role in FA pathway integrity, recruiting FANCM to the site of interstrand cross links, preventing the cells from entering mitosis prematurely, and efficient activation of the CHK1 and G2-M checkpoints.]. 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:23698467
;
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:NP896993.RAhgPIv7Kn4VngYZvJt-pym3gBf6wrboTMzw3ZVgQVGh4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:11+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" .
}