@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP564381.RAPSvjkTznAW89G22hqOCd138BLpqPlm4pIWZqBdPnezw
> .
@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:NP564381.RAPSvjkTznAW89G22hqOCd138BLpqPlm4pIWZqBdPnezw130_head
{
this:
np:hasAssertion
dgn-np:NP564381.RAPSvjkTznAW89G22hqOCd138BLpqPlm4pIWZqBdPnezw130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP564381.RAPSvjkTznAW89G22hqOCd138BLpqPlm4pIWZqBdPnezw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP564381.RAPSvjkTznAW89G22hqOCd138BLpqPlm4pIWZqBdPnezw130_assertion
a
np:Assertion
.
dgn-np:NP564381.RAPSvjkTznAW89G22hqOCd138BLpqPlm4pIWZqBdPnezw130_provenance
a
np:Provenance
.
dgn-np:NP564381.RAPSvjkTznAW89G22hqOCd138BLpqPlm4pIWZqBdPnezw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP564381.RAPSvjkTznAW89G22hqOCd138BLpqPlm4pIWZqBdPnezw130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0008479
a
ncit:C7057
.
dgn-gda:DGN00bd1e79a6248f8a8a5fe0cfeaeb2660
sio:SIO_000628
miriam-gene:7248
,
lld:C0008479
;
a
sio:SIO_001121
.
}
dgn-np:NP564381.RAPSvjkTznAW89G22hqOCd138BLpqPlm4pIWZqBdPnezw130_provenance
{
dgn-np:NP564381.RAPSvjkTznAW89G22hqOCd138BLpqPlm4pIWZqBdPnezw130_assertion
dcterms:description
"[Patterns of EXT gene mutation in hereditary multiple exostoses, in solitary and multiple osteochondromas, and in chondrosarcoma are analogous to those found in other tumour suppressor genes responsible for family cancer traits and associated malignancies.]. 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:10398153
;
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:NP564381.RAPSvjkTznAW89G22hqOCd138BLpqPlm4pIWZqBdPnezw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}