@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs
> .
@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:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_head
{
this:
np:hasAssertion
dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_assertion
;
np:hasProvenance
dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_provenance
;
np:hasPublicationInfo
dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_assertion
a
np:Assertion
.
dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_provenance
a
np:Provenance
.
dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_assertion
{
miriam-gene:11200
a
ncit:C16612
.
lld:C1458155
a
ncit:C7057
.
dgn-gda:DGNf933dfb7dfae2a540395773fed5df692
sio:SIO_000628
miriam-gene:11200
,
lld:C1458155
;
a
sio:SIO_001122
.
}
dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_provenance
{
dgn-np:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_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:NP108448.RAbvR8lEcEFQkiAEJvZrIWm-jclg5AA7I8lJLJv5U1Uzs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:55+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" .
}