@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP168565.RAjFE6zAKVBMkHoq5KEnnkN3hgePHcTUxITFR4sjTx_Tw
> .
@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:NP168565.RAjFE6zAKVBMkHoq5KEnnkN3hgePHcTUxITFR4sjTx_Tw130_head
{
this:
np:hasAssertion
dgn-np:NP168565.RAjFE6zAKVBMkHoq5KEnnkN3hgePHcTUxITFR4sjTx_Tw130_assertion
;
np:hasProvenance
dgn-np:NP168565.RAjFE6zAKVBMkHoq5KEnnkN3hgePHcTUxITFR4sjTx_Tw130_provenance
;
np:hasPublicationInfo
dgn-np:NP168565.RAjFE6zAKVBMkHoq5KEnnkN3hgePHcTUxITFR4sjTx_Tw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP168565.RAjFE6zAKVBMkHoq5KEnnkN3hgePHcTUxITFR4sjTx_Tw130_assertion
a
np:Assertion
.
dgn-np:NP168565.RAjFE6zAKVBMkHoq5KEnnkN3hgePHcTUxITFR4sjTx_Tw130_provenance
a
np:Provenance
.
dgn-np:NP168565.RAjFE6zAKVBMkHoq5KEnnkN3hgePHcTUxITFR4sjTx_Tw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP168565.RAjFE6zAKVBMkHoq5KEnnkN3hgePHcTUxITFR4sjTx_Tw130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0334108
a
ncit:C7057
.
dgn-gda:DGN2991ed98ca4268a36802f73db9b9cd96
sio:SIO_000628
miriam-gene:324
,
lld:C0334108
;
a
sio:SIO_001121
.
}
dgn-np:NP168565.RAjFE6zAKVBMkHoq5KEnnkN3hgePHcTUxITFR4sjTx_Tw130_provenance
{
dgn-np:NP168565.RAjFE6zAKVBMkHoq5KEnnkN3hgePHcTUxITFR4sjTx_Tw130_assertion
dcterms:description
"[Familial adenomatous polyposis, caused by mutations in the adenomatous polyposis coli gene located at chromosome 5q21, is an autosomal dominant syndrome characterized by polyposis of the colon and rectum and nearly 100 percent progression to colorectal 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:16228830
;
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:NP168565.RAjFE6zAKVBMkHoq5KEnnkN3hgePHcTUxITFR4sjTx_Tw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:31+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" .
}