@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP272100.RAdGzWgjMGKBTgOdpwPWZxU_oMIJeFDJlPe5Kx4nLctgQ
> .
@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 dcterms: <
http://purl.org/dc/terms/
> .
@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/v4.0.0/void/
> .
dgn-np:NP272100.RAdGzWgjMGKBTgOdpwPWZxU_oMIJeFDJlPe5Kx4nLctgQ130_head
{
this:
np:hasAssertion
dgn-np:NP272100.RAdGzWgjMGKBTgOdpwPWZxU_oMIJeFDJlPe5Kx4nLctgQ130_assertion
;
np:hasProvenance
dgn-np:NP272100.RAdGzWgjMGKBTgOdpwPWZxU_oMIJeFDJlPe5Kx4nLctgQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP272100.RAdGzWgjMGKBTgOdpwPWZxU_oMIJeFDJlPe5Kx4nLctgQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP272100.RAdGzWgjMGKBTgOdpwPWZxU_oMIJeFDJlPe5Kx4nLctgQ130_assertion
a
np:Assertion
.
dgn-np:NP272100.RAdGzWgjMGKBTgOdpwPWZxU_oMIJeFDJlPe5Kx4nLctgQ130_provenance
a
np:Provenance
.
dgn-np:NP272100.RAdGzWgjMGKBTgOdpwPWZxU_oMIJeFDJlPe5Kx4nLctgQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP272100.RAdGzWgjMGKBTgOdpwPWZxU_oMIJeFDJlPe5Kx4nLctgQ130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN7673e979b55c40f28587e9decdeac25a
sio:SIO_000628
miriam-gene:1029
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP272100.RAdGzWgjMGKBTgOdpwPWZxU_oMIJeFDJlPe5Kx4nLctgQ130_provenance
{
dgn-np:NP272100.RAdGzWgjMGKBTgOdpwPWZxU_oMIJeFDJlPe5Kx4nLctgQ130_assertion
dcterms:description
"[At present, clinical predictive genetic testing for mutations in the CDKN2A gene is available commercially, but its use has been limited by uncertainty as to how test results would affect the management of melanoma-prone family members.]. 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:10630172
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP272100.RAdGzWgjMGKBTgOdpwPWZxU_oMIJeFDJlPe5Kx4nLctgQ130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:49+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}