@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU
> .
@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:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_head
{
this:
np:hasAssertion
dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_assertion
;
np:hasProvenance
dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_provenance
;
np:hasPublicationInfo
dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_assertion
a
np:Assertion
.
dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_provenance
a
np:Provenance
.
dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGN86fda33d06f458791ef4c426f2fce301
sio:SIO_000628
miriam-gene:675
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_provenance
{
dgn-np:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_assertion
dcterms:description
"[As the first effort, we have created a novel variant database of BRCA1 and BRCA2, mismatch repair genes (MMR), and APC genes for breast cancer, Lynch syndrome, and familial adenomatous polyposis (FAP), respectively, in the Chinese population using the Leiden Open Variation Database (LOVD) format.]. 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:21901790
;
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:NP771281.RApPgP8Ni4S09RrGNGwYZv5930WRcYeM3p5xbG96jLgHU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:46+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" .
}