@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw
> .
@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:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_head
{
this:
np:hasAssertion
dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_assertion
;
np:hasProvenance
dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_provenance
;
np:hasPublicationInfo
dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_assertion
a
np:Assertion
.
dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_provenance
a
np:Provenance
.
dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_assertion
{
miriam-gene:2131
a
ncit:C16612
.
lld:C0206641
a
ncit:C7057
.
dgn-gda:DGN3a35b09a053cfe8f97d18af4677693aa
sio:SIO_000628
miriam-gene:2131
,
lld:C0206641
;
a
sio:SIO_001121
.
}
dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_provenance
{
dgn-np:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_assertion
dcterms:description
"[The genetics of these tumors is intriguing ranging from single gene event (ie, EXT mutation in multiple osteochondromas) to heterogeneous rearrangements with no recurrent involved chromosomal regions such as in chondroblastoma.]. 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:19700940
;
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:NP224989.RAS7zszcZHPEF_FibHBBNFWmVfqeRrGEXh-BSgpilHRQw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:05+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" .
}