@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP299022.RAn3ULCpB83_EfrqbvFUcd8okh7SeEpoB_Lg_ZusbgPS0
> .
@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:NP299022.RAn3ULCpB83_EfrqbvFUcd8okh7SeEpoB_Lg_ZusbgPS0130_head
{
this:
np:hasAssertion
dgn-np:NP299022.RAn3ULCpB83_EfrqbvFUcd8okh7SeEpoB_Lg_ZusbgPS0130_assertion
;
np:hasProvenance
dgn-np:NP299022.RAn3ULCpB83_EfrqbvFUcd8okh7SeEpoB_Lg_ZusbgPS0130_provenance
;
np:hasPublicationInfo
dgn-np:NP299022.RAn3ULCpB83_EfrqbvFUcd8okh7SeEpoB_Lg_ZusbgPS0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP299022.RAn3ULCpB83_EfrqbvFUcd8okh7SeEpoB_Lg_ZusbgPS0130_assertion
a
np:Assertion
.
dgn-np:NP299022.RAn3ULCpB83_EfrqbvFUcd8okh7SeEpoB_Lg_ZusbgPS0130_provenance
a
np:Provenance
.
dgn-np:NP299022.RAn3ULCpB83_EfrqbvFUcd8okh7SeEpoB_Lg_ZusbgPS0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP299022.RAn3ULCpB83_EfrqbvFUcd8okh7SeEpoB_Lg_ZusbgPS0130_assertion
{
miriam-gene:5395
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN7f594a5e23871fa9ba7cc02a447c8c2e
sio:SIO_000628
miriam-gene:5395
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP299022.RAn3ULCpB83_EfrqbvFUcd8okh7SeEpoB_Lg_ZusbgPS0130_provenance
{
dgn-np:NP299022.RAn3ULCpB83_EfrqbvFUcd8okh7SeEpoB_Lg_ZusbgPS0130_assertion
dcterms:description
"[The discipline of molecular genetics has identified germline mutations that include APC in familial adenomatous polyposis (FAP) and mutator genes, namely MSH2, MLH1, PMS1, and PMS2 in hereditary nonpolyposis colorectal cancer (HNPCC).]. 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:9062584
;
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:NP299022.RAn3ULCpB83_EfrqbvFUcd8okh7SeEpoB_Lg_ZusbgPS0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:50+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" .
}