@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP148188.RAzr0MBmGZiXfXMmx8AZ9vv0-G6wf6pKLfbKVytRV9ngo
> .
@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:NP148188.RAzr0MBmGZiXfXMmx8AZ9vv0-G6wf6pKLfbKVytRV9ngo130_head
{
this:
np:hasAssertion
dgn-np:NP148188.RAzr0MBmGZiXfXMmx8AZ9vv0-G6wf6pKLfbKVytRV9ngo130_assertion
;
np:hasProvenance
dgn-np:NP148188.RAzr0MBmGZiXfXMmx8AZ9vv0-G6wf6pKLfbKVytRV9ngo130_provenance
;
np:hasPublicationInfo
dgn-np:NP148188.RAzr0MBmGZiXfXMmx8AZ9vv0-G6wf6pKLfbKVytRV9ngo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP148188.RAzr0MBmGZiXfXMmx8AZ9vv0-G6wf6pKLfbKVytRV9ngo130_assertion
a
np:Assertion
.
dgn-np:NP148188.RAzr0MBmGZiXfXMmx8AZ9vv0-G6wf6pKLfbKVytRV9ngo130_provenance
a
np:Provenance
.
dgn-np:NP148188.RAzr0MBmGZiXfXMmx8AZ9vv0-G6wf6pKLfbKVytRV9ngo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP148188.RAzr0MBmGZiXfXMmx8AZ9vv0-G6wf6pKLfbKVytRV9ngo130_assertion
{
miriam-gene:11200
a
ncit:C16612
.
lld:C0085390
a
ncit:C7057
.
dgn-gda:DGN616576adfecc8561049240e04edb743d
sio:SIO_000628
miriam-gene:11200
,
lld:C0085390
;
a
sio:SIO_001122
.
}
dgn-np:NP148188.RAzr0MBmGZiXfXMmx8AZ9vv0-G6wf6pKLfbKVytRV9ngo130_provenance
{
dgn-np:NP148188.RAzr0MBmGZiXfXMmx8AZ9vv0-G6wf6pKLfbKVytRV9ngo130_assertion
dcterms:description
"[We believe that CHEK2 mutations are not associated with the cancer types seen in the LFS or LFL (other than breast cancer) and it is no longer reasonable to consider CHEK2 mutations to be a cause of LFS (Li-Fraumeni syndrome).]. 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:18178638
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP148188.RAzr0MBmGZiXfXMmx8AZ9vv0-G6wf6pKLfbKVytRV9ngo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:17+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" .
}