@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP415822.RAonMaGRdRrRlUwQDzhcIfr2x2aixgL_BWi4_F-FOCpA8
> .
@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:NP415822.RAonMaGRdRrRlUwQDzhcIfr2x2aixgL_BWi4_F-FOCpA8130_head
{
this:
np:hasAssertion
dgn-np:NP415822.RAonMaGRdRrRlUwQDzhcIfr2x2aixgL_BWi4_F-FOCpA8130_assertion
;
np:hasProvenance
dgn-np:NP415822.RAonMaGRdRrRlUwQDzhcIfr2x2aixgL_BWi4_F-FOCpA8130_provenance
;
np:hasPublicationInfo
dgn-np:NP415822.RAonMaGRdRrRlUwQDzhcIfr2x2aixgL_BWi4_F-FOCpA8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP415822.RAonMaGRdRrRlUwQDzhcIfr2x2aixgL_BWi4_F-FOCpA8130_assertion
a
np:Assertion
.
dgn-np:NP415822.RAonMaGRdRrRlUwQDzhcIfr2x2aixgL_BWi4_F-FOCpA8130_provenance
a
np:Provenance
.
dgn-np:NP415822.RAonMaGRdRrRlUwQDzhcIfr2x2aixgL_BWi4_F-FOCpA8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP415822.RAonMaGRdRrRlUwQDzhcIfr2x2aixgL_BWi4_F-FOCpA8130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C1333600
a
ncit:C7057
.
dgn-gda:DGN30d8b0c31850f340335c7cb2ab7947ba
sio:SIO_000628
miriam-gene:5624
,
lld:C1333600
;
a
sio:SIO_001121
.
}
dgn-np:NP415822.RAonMaGRdRrRlUwQDzhcIfr2x2aixgL_BWi4_F-FOCpA8130_provenance
{
dgn-np:NP415822.RAonMaGRdRrRlUwQDzhcIfr2x2aixgL_BWi4_F-FOCpA8130_assertion
dcterms:description
"[The associated familial cancer susceptibility syndromes are familial adenomatous polyposis coli, due to inherited APC mutations, and Lynch Syndrome or hereditary nonpolyposis colorectal cancer syndrome, due to inherited mutations in one of the mismatch repair genes (predominantly MLH1 and MSH2).]. 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:23417071
;
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:NP415822.RAonMaGRdRrRlUwQDzhcIfr2x2aixgL_BWi4_F-FOCpA8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:07+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" .
}