@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP830124.RAM4JXmjrC2GQvfcp4ozEXkDmhBrno8Sd_iUO189q0FDk
> .
@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:NP830124.RAM4JXmjrC2GQvfcp4ozEXkDmhBrno8Sd_iUO189q0FDk130_head
{
this:
np:hasAssertion
dgn-np:NP830124.RAM4JXmjrC2GQvfcp4ozEXkDmhBrno8Sd_iUO189q0FDk130_assertion
;
np:hasProvenance
dgn-np:NP830124.RAM4JXmjrC2GQvfcp4ozEXkDmhBrno8Sd_iUO189q0FDk130_provenance
;
np:hasPublicationInfo
dgn-np:NP830124.RAM4JXmjrC2GQvfcp4ozEXkDmhBrno8Sd_iUO189q0FDk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP830124.RAM4JXmjrC2GQvfcp4ozEXkDmhBrno8Sd_iUO189q0FDk130_assertion
a
np:Assertion
.
dgn-np:NP830124.RAM4JXmjrC2GQvfcp4ozEXkDmhBrno8Sd_iUO189q0FDk130_provenance
a
np:Provenance
.
dgn-np:NP830124.RAM4JXmjrC2GQvfcp4ozEXkDmhBrno8Sd_iUO189q0FDk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP830124.RAM4JXmjrC2GQvfcp4ozEXkDmhBrno8Sd_iUO189q0FDk130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGNcf794cb761b947e3b7f53c2fa09a5278
sio:SIO_000628
miriam-gene:675
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP830124.RAM4JXmjrC2GQvfcp4ozEXkDmhBrno8Sd_iUO189q0FDk130_provenance
{
dgn-np:NP830124.RAM4JXmjrC2GQvfcp4ozEXkDmhBrno8Sd_iUO189q0FDk130_assertion
dcterms:description
"[First, the impact of highly penetrant but lowly prevalent mutations of germline DNA on cancer prognosis has been studied extensively for BRCA1 and BRCA2 mutations as well as mutations related to hereditary nonpolyposis colorectal cancer syndrome.]. 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:20679599
;
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:NP830124.RAM4JXmjrC2GQvfcp4ozEXkDmhBrno8Sd_iUO189q0FDk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:01+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" .
}