@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY
> .
@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:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_head
{
this:
np:hasAssertion
dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_assertion
;
np:hasProvenance
dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_provenance
;
np:hasPublicationInfo
dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_assertion
a
np:Assertion
.
dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_provenance
a
np:Provenance
.
dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0037579
a
ncit:C7057
.
dgn-gda:DGN5e11cdcce59ebdc9f6cebd9d6bfd0ab3
sio:SIO_000628
miriam-gene:7157
,
lld:C0037579
;
a
sio:SIO_001121
.
}
dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_provenance
{
dgn-np:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_assertion
dcterms:description
"[The p53 tumor suppressor gene is a possible candidate underlying the syndrome because (a) mutations in the p53 gene are ubiquitous in human cancer, including colon carcinoma and gliomas, and (b) somatic or germ line mutations of the p53 tumor suppressor gene cause the Li-Fraumeni syndrome, which is characterized by the association of breast and soft tissue tumors.]. 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:8439970
;
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:NP419284.RAodphZ4QLPOrF4WWXn6K3W3QZMWHKCLL81DABB-HebzY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:09+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" .
}