@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP70921.RAG58idWTbWvFub45U7z_Sua0iYJ09lx__PUmSqyGkcuc
> .
@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:NP70921.RAG58idWTbWvFub45U7z_Sua0iYJ09lx__PUmSqyGkcuc130_head
{
this:
np:hasAssertion
dgn-np:NP70921.RAG58idWTbWvFub45U7z_Sua0iYJ09lx__PUmSqyGkcuc130_assertion
;
np:hasProvenance
dgn-np:NP70921.RAG58idWTbWvFub45U7z_Sua0iYJ09lx__PUmSqyGkcuc130_provenance
;
np:hasPublicationInfo
dgn-np:NP70921.RAG58idWTbWvFub45U7z_Sua0iYJ09lx__PUmSqyGkcuc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP70921.RAG58idWTbWvFub45U7z_Sua0iYJ09lx__PUmSqyGkcuc130_assertion
a
np:Assertion
.
dgn-np:NP70921.RAG58idWTbWvFub45U7z_Sua0iYJ09lx__PUmSqyGkcuc130_provenance
a
np:Provenance
.
dgn-np:NP70921.RAG58idWTbWvFub45U7z_Sua0iYJ09lx__PUmSqyGkcuc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP70921.RAG58idWTbWvFub45U7z_Sua0iYJ09lx__PUmSqyGkcuc130_assertion
{
miriam-gene:3265
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN33f3ae6a79a76a21c57afe85a8a73a45
sio:SIO_000628
miriam-gene:3265
,
lld:C1527249
;
a
sio:SIO_001122
.
}
dgn-np:NP70921.RAG58idWTbWvFub45U7z_Sua0iYJ09lx__PUmSqyGkcuc130_provenance
{
dgn-np:NP70921.RAG58idWTbWvFub45U7z_Sua0iYJ09lx__PUmSqyGkcuc130_assertion
dcterms:description
"[ APC-I1307K, HRAS1-VNTR, and MTHFR variants represent the strongest candidates for low penetrance susceptibility alleles identified to date. Although their genotypic risks are modest, their high frequency in the population implies that they may well have ]. 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:11487538
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP70921.RAG58idWTbWvFub45U7z_Sua0iYJ09lx__PUmSqyGkcuc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:42:20+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" .
}