@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg
> .
@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:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_head
{
this:
np:hasAssertion
dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_assertion
;
np:hasProvenance
dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_provenance
;
np:hasPublicationInfo
dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_assertion
a
np:Assertion
.
dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_provenance
a
np:Provenance
.
dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0751623
a
ncit:C7057
.
dgn-gda:DGN6f02f8ba6aab7ec46392d1cd3dc90f92
sio:SIO_000628
miriam-gene:7157
,
lld:C0751623
;
a
sio:SIO_001121
.
}
dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_provenance
{
dgn-np:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_assertion
dcterms:description
"[We investigated the possibility that p53 mutations in the germline are associated with second primary cancers that arise in children and young adults who would not be considered as belonging to Li-Fraumeni families.]. 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:1565144
;
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:NP877307.RAGiZ7hvZxu9MQ5XNNILHGJQDryr700tjKJz1HWdf55Eg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:56+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" .
}