@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP970769.RAdCrMKJacU7bvQHAxqH2ysiRZJVe9jRxzVVhCEE7eElo
> .
@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:NP970769.RAdCrMKJacU7bvQHAxqH2ysiRZJVe9jRxzVVhCEE7eElo130_head
{
this:
np:hasAssertion
dgn-np:NP970769.RAdCrMKJacU7bvQHAxqH2ysiRZJVe9jRxzVVhCEE7eElo130_assertion
;
np:hasProvenance
dgn-np:NP970769.RAdCrMKJacU7bvQHAxqH2ysiRZJVe9jRxzVVhCEE7eElo130_provenance
;
np:hasPublicationInfo
dgn-np:NP970769.RAdCrMKJacU7bvQHAxqH2ysiRZJVe9jRxzVVhCEE7eElo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP970769.RAdCrMKJacU7bvQHAxqH2ysiRZJVe9jRxzVVhCEE7eElo130_assertion
a
np:Assertion
.
dgn-np:NP970769.RAdCrMKJacU7bvQHAxqH2ysiRZJVe9jRxzVVhCEE7eElo130_provenance
a
np:Provenance
.
dgn-np:NP970769.RAdCrMKJacU7bvQHAxqH2ysiRZJVe9jRxzVVhCEE7eElo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP970769.RAdCrMKJacU7bvQHAxqH2ysiRZJVe9jRxzVVhCEE7eElo130_assertion
{
miriam-gene:2956
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN7f73e945d7c0f0ccbd6b908d4e307b1e
sio:SIO_000628
miriam-gene:2956
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP970769.RAdCrMKJacU7bvQHAxqH2ysiRZJVe9jRxzVVhCEE7eElo130_provenance
{
dgn-np:NP970769.RAdCrMKJacU7bvQHAxqH2ysiRZJVe9jRxzVVhCEE7eElo130_assertion
dcterms:description
"[Germ line mutations in genes involved in hereditary cancer syndromes, such as BRCA1 and BRCA2 in breast cancer and MSH2, MSH6, MLH1, and PSM2 in hereditary nonpolyposis colorectal cancer (HNPCC, more recently indicated as Lynch syndrome), confer a high risk to develop 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:22454054
;
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:NP970769.RAdCrMKJacU7bvQHAxqH2ysiRZJVe9jRxzVVhCEE7eElo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:04+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" .
}