@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP186018.RAuKUM1LWFkbsjuyWW3xcRKJzqSSA1uRXpTHuR8W48fYU
> .
@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:NP186018.RAuKUM1LWFkbsjuyWW3xcRKJzqSSA1uRXpTHuR8W48fYU130_head
{
this:
np:hasAssertion
dgn-np:NP186018.RAuKUM1LWFkbsjuyWW3xcRKJzqSSA1uRXpTHuR8W48fYU130_assertion
;
np:hasProvenance
dgn-np:NP186018.RAuKUM1LWFkbsjuyWW3xcRKJzqSSA1uRXpTHuR8W48fYU130_provenance
;
np:hasPublicationInfo
dgn-np:NP186018.RAuKUM1LWFkbsjuyWW3xcRKJzqSSA1uRXpTHuR8W48fYU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP186018.RAuKUM1LWFkbsjuyWW3xcRKJzqSSA1uRXpTHuR8W48fYU130_assertion
a
np:Assertion
.
dgn-np:NP186018.RAuKUM1LWFkbsjuyWW3xcRKJzqSSA1uRXpTHuR8W48fYU130_provenance
a
np:Provenance
.
dgn-np:NP186018.RAuKUM1LWFkbsjuyWW3xcRKJzqSSA1uRXpTHuR8W48fYU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP186018.RAuKUM1LWFkbsjuyWW3xcRKJzqSSA1uRXpTHuR8W48fYU130_assertion
{
miriam-gene:9968
a
ncit:C16612
.
lld:C0042133
a
ncit:C7057
.
dgn-gda:DGN3bda3a3743315588e7b1d8c151a42013
sio:SIO_000628
miriam-gene:9968
,
lld:C0042133
;
a
sio:SIO_001121
.
}
dgn-np:NP186018.RAuKUM1LWFkbsjuyWW3xcRKJzqSSA1uRXpTHuR8W48fYU130_provenance
{
dgn-np:NP186018.RAuKUM1LWFkbsjuyWW3xcRKJzqSSA1uRXpTHuR8W48fYU130_assertion
dcterms:description
"[The complete lack of novel driver point mutations in the examined series highlights the unique role of MED12 mutations in genesis of uterine leiomyomas, and suggests that these mutations alone may be sufficient for tumor development.]. 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:23913526
;
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:NP186018.RAuKUM1LWFkbsjuyWW3xcRKJzqSSA1uRXpTHuR8W48fYU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:42+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" .
}