@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP560618.RA6ES-6Aa2KKidY-9Q4lhvxnVrntgUP-ahlkXjblxk3Rk
> .
@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:NP560618.RA6ES-6Aa2KKidY-9Q4lhvxnVrntgUP-ahlkXjblxk3Rk130_head
{
this:
np:hasAssertion
dgn-np:NP560618.RA6ES-6Aa2KKidY-9Q4lhvxnVrntgUP-ahlkXjblxk3Rk130_assertion
;
np:hasProvenance
dgn-np:NP560618.RA6ES-6Aa2KKidY-9Q4lhvxnVrntgUP-ahlkXjblxk3Rk130_provenance
;
np:hasPublicationInfo
dgn-np:NP560618.RA6ES-6Aa2KKidY-9Q4lhvxnVrntgUP-ahlkXjblxk3Rk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP560618.RA6ES-6Aa2KKidY-9Q4lhvxnVrntgUP-ahlkXjblxk3Rk130_assertion
a
np:Assertion
.
dgn-np:NP560618.RA6ES-6Aa2KKidY-9Q4lhvxnVrntgUP-ahlkXjblxk3Rk130_provenance
a
np:Provenance
.
dgn-np:NP560618.RA6ES-6Aa2KKidY-9Q4lhvxnVrntgUP-ahlkXjblxk3Rk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP560618.RA6ES-6Aa2KKidY-9Q4lhvxnVrntgUP-ahlkXjblxk3Rk130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C0027672
a
ncit:C7057
.
dgn-gda:DGNf2390cb60153534598545af7a1a2c6e9
sio:SIO_000628
miriam-gene:672
,
lld:C0027672
;
a
sio:SIO_001121
.
}
dgn-np:NP560618.RA6ES-6Aa2KKidY-9Q4lhvxnVrntgUP-ahlkXjblxk3Rk130_provenance
{
dgn-np:NP560618.RA6ES-6Aa2KKidY-9Q4lhvxnVrntgUP-ahlkXjblxk3Rk130_assertion
dcterms:description
"[The objectives of this study were to estimate the proportion of unselected pancreatic cancer patients belonging to hereditary cancer syndrome families and to determine the frequency ofp16, BRCA1, BRCA2, hMSH2, and hMLH1 germ-line mutations in patients with a personal or family history of cancer.]. 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:10667595
;
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:NP560618.RA6ES-6Aa2KKidY-9Q4lhvxnVrntgUP-ahlkXjblxk3Rk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:38+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" .
}