@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP938584.RAIJ8yAus6r2YugUV3l1JeGavs3-9XCYQWMz38IicWAeg
> .
@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:NP938584.RAIJ8yAus6r2YugUV3l1JeGavs3-9XCYQWMz38IicWAeg130_head
{
this:
np:hasAssertion
dgn-np:NP938584.RAIJ8yAus6r2YugUV3l1JeGavs3-9XCYQWMz38IicWAeg130_assertion
;
np:hasProvenance
dgn-np:NP938584.RAIJ8yAus6r2YugUV3l1JeGavs3-9XCYQWMz38IicWAeg130_provenance
;
np:hasPublicationInfo
dgn-np:NP938584.RAIJ8yAus6r2YugUV3l1JeGavs3-9XCYQWMz38IicWAeg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP938584.RAIJ8yAus6r2YugUV3l1JeGavs3-9XCYQWMz38IicWAeg130_assertion
a
np:Assertion
.
dgn-np:NP938584.RAIJ8yAus6r2YugUV3l1JeGavs3-9XCYQWMz38IicWAeg130_provenance
a
np:Provenance
.
dgn-np:NP938584.RAIJ8yAus6r2YugUV3l1JeGavs3-9XCYQWMz38IicWAeg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP938584.RAIJ8yAus6r2YugUV3l1JeGavs3-9XCYQWMz38IicWAeg130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C1458156
a
ncit:C7057
.
dgn-gda:DGNdd4e324922f1c808dd6eaecd1f53c60f
sio:SIO_000628
miriam-gene:5979
,
lld:C1458156
;
a
sio:SIO_001121
.
}
dgn-np:NP938584.RAIJ8yAus6r2YugUV3l1JeGavs3-9XCYQWMz38IicWAeg130_provenance
{
dgn-np:NP938584.RAIJ8yAus6r2YugUV3l1JeGavs3-9XCYQWMz38IicWAeg130_assertion
dcterms:description
"[The study of RET-CDS mutations that appear de novo is essential not only for understanding the mechanistic of the disease but also for penetrance and recurrence risk estimations, being the ultimate goal for the improvement in disease management and counseling.]. 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:22131258
;
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:NP938584.RAIJ8yAus6r2YugUV3l1JeGavs3-9XCYQWMz38IicWAeg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:35+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" .
}