@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP580910.RAImCKir2k-zsbbO8ELEhAsAf-Pr7-6W8FKe8p4y4zCE8
> .
@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:NP580910.RAImCKir2k-zsbbO8ELEhAsAf-Pr7-6W8FKe8p4y4zCE8130_head
{
this:
np:hasAssertion
dgn-np:NP580910.RAImCKir2k-zsbbO8ELEhAsAf-Pr7-6W8FKe8p4y4zCE8130_assertion
;
np:hasProvenance
dgn-np:NP580910.RAImCKir2k-zsbbO8ELEhAsAf-Pr7-6W8FKe8p4y4zCE8130_provenance
;
np:hasPublicationInfo
dgn-np:NP580910.RAImCKir2k-zsbbO8ELEhAsAf-Pr7-6W8FKe8p4y4zCE8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP580910.RAImCKir2k-zsbbO8ELEhAsAf-Pr7-6W8FKe8p4y4zCE8130_assertion
a
np:Assertion
.
dgn-np:NP580910.RAImCKir2k-zsbbO8ELEhAsAf-Pr7-6W8FKe8p4y4zCE8130_provenance
a
np:Provenance
.
dgn-np:NP580910.RAImCKir2k-zsbbO8ELEhAsAf-Pr7-6W8FKe8p4y4zCE8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP580910.RAImCKir2k-zsbbO8ELEhAsAf-Pr7-6W8FKe8p4y4zCE8130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C2751492
a
ncit:C7057
.
dgn-gda:DGN4f040e1c07f151d6abe6d7f4ea656fbe
sio:SIO_000628
miriam-gene:4292
,
lld:C2751492
;
a
sio:SIO_001121
.
}
dgn-np:NP580910.RAImCKir2k-zsbbO8ELEhAsAf-Pr7-6W8FKe8p4y4zCE8130_provenance
{
dgn-np:NP580910.RAImCKir2k-zsbbO8ELEhAsAf-Pr7-6W8FKe8p4y4zCE8130_assertion
dcterms:description
"[The genes that give rise to the rare syndromes of FAP and HNPCC are now known and current research is addressing the cellular mechanisms of these genes and the proper application of genetic testing in families with one of the syndromes.]. 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:10709679
;
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:NP580910.RAImCKir2k-zsbbO8ELEhAsAf-Pr7-6W8FKe8p4y4zCE8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:50+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" .
}