@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP514772.RAsST_5YQUjXP7nPDe_SxgOllqxNrCwuNXVvVoM4cfEww
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP514772.RAsST_5YQUjXP7nPDe_SxgOllqxNrCwuNXVvVoM4cfEww130_head
{
this:
np:hasAssertion
dgn-np:NP514772.RAsST_5YQUjXP7nPDe_SxgOllqxNrCwuNXVvVoM4cfEww130_assertion
;
np:hasProvenance
dgn-np:NP514772.RAsST_5YQUjXP7nPDe_SxgOllqxNrCwuNXVvVoM4cfEww130_provenance
;
np:hasPublicationInfo
dgn-np:NP514772.RAsST_5YQUjXP7nPDe_SxgOllqxNrCwuNXVvVoM4cfEww130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP514772.RAsST_5YQUjXP7nPDe_SxgOllqxNrCwuNXVvVoM4cfEww130_assertion
a
np:Assertion
.
dgn-np:NP514772.RAsST_5YQUjXP7nPDe_SxgOllqxNrCwuNXVvVoM4cfEww130_provenance
a
np:Provenance
.
dgn-np:NP514772.RAsST_5YQUjXP7nPDe_SxgOllqxNrCwuNXVvVoM4cfEww130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP514772.RAsST_5YQUjXP7nPDe_SxgOllqxNrCwuNXVvVoM4cfEww130_assertion
{
miriam-gene:472
a
ncit:C16612
.
lld:C0004135
a
ncit:C7057
.
dgn-gda:DGN626df4ca72b4f1a8b6f38296a1b92d3f
sio:SIO_000628
miriam-gene:472
,
lld:C0004135
;
a
sio:SIO_001121
.
}
dgn-np:NP514772.RAsST_5YQUjXP7nPDe_SxgOllqxNrCwuNXVvVoM4cfEww130_provenance
{
dgn-np:NP514772.RAsST_5YQUjXP7nPDe_SxgOllqxNrCwuNXVvVoM4cfEww130_assertion
dcterms:description
"[The risk of BC was higher in ATM heterozygous (HetATM) women and did not differ significantly according to the type of ATM mutation (missense vs truncating) carried by the AT family members but appeared associated with the position of some truncating mutations in certain binding domains of the ATM protein.]. 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:16180724
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP514772.RAsST_5YQUjXP7nPDe_SxgOllqxNrCwuNXVvVoM4cfEww130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:38+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}