@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8
> .
@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 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:NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_head
{
this:
np:hasAssertion
dgn-np:NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_assertion
;
np:hasProvenance
dgn-np:NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_provenance
;
np:hasPublicationInfo
dgn-np:NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_assertion
a
np:Assertion
.
dgn-np:NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_provenance
a
np:Provenance
.
dgn-np:NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0085183
a
ncit:C7057
.
dgn-gda:DGNd7a0af9ac471accf5af41500b6e3f079
sio:SIO_000628
miriam-gene:7157
,
lld:C0085183
;
a
sio:SIO_001121
.
}
dgn-np:NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_provenance
{
dgn-np:NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_assertion
dc:description
"[Germline p53 gene mutations were detected in six of 19 patients with multifocal glioma, including two with family history of cancer, one with another primary malignancy, and two with all three risk factors; one of four patients with unifocal glioma, another primary malignancy, and a family history of cancer; and two of 15 patients with unifocal glioma and a family history of cancer but no second malignancies.]. 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:8308926
;
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:NP377119.RAAoVmwh7dPDqDRn5kwXLYt1IeI9oJD1nQxlCt5j74WK8130_publicationInfo
{
this:
dc:created
"2014-10-02T12:35:40+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}