@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP218324.RA-PVxjEMP5USz1T8JGKopR2PcjWduRzs2lxxiHhdxTCU
> .
@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:NP218324.RA-PVxjEMP5USz1T8JGKopR2PcjWduRzs2lxxiHhdxTCU130_head
{
this:
np:hasAssertion
dgn-np:NP218324.RA-PVxjEMP5USz1T8JGKopR2PcjWduRzs2lxxiHhdxTCU130_assertion
;
np:hasProvenance
dgn-np:NP218324.RA-PVxjEMP5USz1T8JGKopR2PcjWduRzs2lxxiHhdxTCU130_provenance
;
np:hasPublicationInfo
dgn-np:NP218324.RA-PVxjEMP5USz1T8JGKopR2PcjWduRzs2lxxiHhdxTCU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP218324.RA-PVxjEMP5USz1T8JGKopR2PcjWduRzs2lxxiHhdxTCU130_assertion
a
np:Assertion
.
dgn-np:NP218324.RA-PVxjEMP5USz1T8JGKopR2PcjWduRzs2lxxiHhdxTCU130_provenance
a
np:Provenance
.
dgn-np:NP218324.RA-PVxjEMP5USz1T8JGKopR2PcjWduRzs2lxxiHhdxTCU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP218324.RA-PVxjEMP5USz1T8JGKopR2PcjWduRzs2lxxiHhdxTCU130_assertion
{
miriam-gene:10923
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN33b72bcb32a1aa6663fe9ca0ace85eee
sio:SIO_000628
miriam-gene:10923
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP218324.RA-PVxjEMP5USz1T8JGKopR2PcjWduRzs2lxxiHhdxTCU130_provenance
{
dgn-np:NP218324.RA-PVxjEMP5USz1T8JGKopR2PcjWduRzs2lxxiHhdxTCU130_assertion
dcterms:description
"[The lack of complete concordance between p15 and p16 expression implies that the genes are not functionally redundant and that loss of either gene may be important in the pathogenesis of MM.]. 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:8873047
;
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:NP218324.RA-PVxjEMP5USz1T8JGKopR2PcjWduRzs2lxxiHhdxTCU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:01+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" .
}