@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1022.RALKvuWJJRzJA8xR_G-8A_zH0erQngWVVxT6CfEjrdoX0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP1022.RALKvuWJJRzJA8xR_G-8A_zH0erQngWVVxT6CfEjrdoX0130_head
{
this:
np:hasAssertion
dgn-np:NP1022.RALKvuWJJRzJA8xR_G-8A_zH0erQngWVVxT6CfEjrdoX0130_assertion
;
np:hasProvenance
dgn-np:NP1022.RALKvuWJJRzJA8xR_G-8A_zH0erQngWVVxT6CfEjrdoX0130_provenance
;
np:hasPublicationInfo
dgn-np:NP1022.RALKvuWJJRzJA8xR_G-8A_zH0erQngWVVxT6CfEjrdoX0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1022.RALKvuWJJRzJA8xR_G-8A_zH0erQngWVVxT6CfEjrdoX0130_assertion
a
np:Assertion
.
dgn-np:NP1022.RALKvuWJJRzJA8xR_G-8A_zH0erQngWVVxT6CfEjrdoX0130_provenance
a
np:Provenance
.
dgn-np:NP1022.RALKvuWJJRzJA8xR_G-8A_zH0erQngWVVxT6CfEjrdoX0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1022.RALKvuWJJRzJA8xR_G-8A_zH0erQngWVVxT6CfEjrdoX0130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C1835398
a
ncit:C7057
.
dgn-gda:DGNf90f47d941250c2d1803ea877ff4a579
sio:SIO_000628
miriam-gene:7157
,
lld:C1835398
;
a
sio:SIO_001122
.
}
dgn-np:NP1022.RALKvuWJJRzJA8xR_G-8A_zH0erQngWVVxT6CfEjrdoX0130_provenance
{
dgn-np:NP1022.RALKvuWJJRzJA8xR_G-8A_zH0erQngWVVxT6CfEjrdoX0130_assertion
dc:description
"[The frequency of germ line p53 mutations can now be examined in additional families with LFS, and in other cancer patients and families with clinical features that might be attributed to the mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:1978757
;
prov:wasDerivedFrom
dgn-void:uniprot-20150221
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
dgn-void:uniprot-20150221
pav:importedOn
"2015-02-21"^^
xsd:date
.
}
dgn-np:NP1022.RALKvuWJJRzJA8xR_G-8A_zH0erQngWVVxT6CfEjrdoX0130_publicationInfo
{
this:
dc:created
"2015-08-25T14:37:42+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:disgenetv3.0rdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}