@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP604068.RAKNlxKXKEYE6qTfTCo5Q5JNidU8qGll40Odp0ekkqhU8
> .
@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:NP604068.RAKNlxKXKEYE6qTfTCo5Q5JNidU8qGll40Odp0ekkqhU8130_head
{
this:
np:hasAssertion
dgn-np:NP604068.RAKNlxKXKEYE6qTfTCo5Q5JNidU8qGll40Odp0ekkqhU8130_assertion
;
np:hasProvenance
dgn-np:NP604068.RAKNlxKXKEYE6qTfTCo5Q5JNidU8qGll40Odp0ekkqhU8130_provenance
;
np:hasPublicationInfo
dgn-np:NP604068.RAKNlxKXKEYE6qTfTCo5Q5JNidU8qGll40Odp0ekkqhU8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP604068.RAKNlxKXKEYE6qTfTCo5Q5JNidU8qGll40Odp0ekkqhU8130_assertion
a
np:Assertion
.
dgn-np:NP604068.RAKNlxKXKEYE6qTfTCo5Q5JNidU8qGll40Odp0ekkqhU8130_provenance
a
np:Provenance
.
dgn-np:NP604068.RAKNlxKXKEYE6qTfTCo5Q5JNidU8qGll40Odp0ekkqhU8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP604068.RAKNlxKXKEYE6qTfTCo5Q5JNidU8qGll40Odp0ekkqhU8130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNafb038ef06822625d226325c00704cc2
sio:SIO_000628
miriam-gene:7157
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP604068.RAKNlxKXKEYE6qTfTCo5Q5JNidU8qGll40Odp0ekkqhU8130_provenance
{
dgn-np:NP604068.RAKNlxKXKEYE6qTfTCo5Q5JNidU8qGll40Odp0ekkqhU8130_assertion
dcterms:description
"[Certain rare, familial mutations in the ATM, BRCA1, BRCA2, CHEK2 or TP53 genes increase susceptibility to breast cancer but it has not, until now, been clear whether common polymorphic variants in the same genes also increase risk.]. 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:17428325
;
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:NP604068.RAKNlxKXKEYE6qTfTCo5Q5JNidU8qGll40Odp0ekkqhU8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:19+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" .
}