@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP559745.RAMCmcRddl0eUl9rMjJXcInOrhh-hHLo3iBdzm-clC6TE
> .
@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:NP559745.RAMCmcRddl0eUl9rMjJXcInOrhh-hHLo3iBdzm-clC6TE130_head
{
this:
np:hasAssertion
dgn-np:NP559745.RAMCmcRddl0eUl9rMjJXcInOrhh-hHLo3iBdzm-clC6TE130_assertion
;
np:hasProvenance
dgn-np:NP559745.RAMCmcRddl0eUl9rMjJXcInOrhh-hHLo3iBdzm-clC6TE130_provenance
;
np:hasPublicationInfo
dgn-np:NP559745.RAMCmcRddl0eUl9rMjJXcInOrhh-hHLo3iBdzm-clC6TE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP559745.RAMCmcRddl0eUl9rMjJXcInOrhh-hHLo3iBdzm-clC6TE130_assertion
a
np:Assertion
.
dgn-np:NP559745.RAMCmcRddl0eUl9rMjJXcInOrhh-hHLo3iBdzm-clC6TE130_provenance
a
np:Provenance
.
dgn-np:NP559745.RAMCmcRddl0eUl9rMjJXcInOrhh-hHLo3iBdzm-clC6TE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP559745.RAMCmcRddl0eUl9rMjJXcInOrhh-hHLo3iBdzm-clC6TE130_assertion
{
miriam-gene:5973
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGN06eb9fec789948250b600de14876562c
sio:SIO_000628
miriam-gene:5973
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP559745.RAMCmcRddl0eUl9rMjJXcInOrhh-hHLo3iBdzm-clC6TE130_provenance
{
dgn-np:NP559745.RAMCmcRddl0eUl9rMjJXcInOrhh-hHLo3iBdzm-clC6TE130_assertion
dcterms:description
"[The author proposes a genetic mechanism on how abnormal function of RBP can result or contribute to the development of human skin cancer and propose an explanation for this association between MMD and cutaneous carcinogenesis.]. 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:19902230
;
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:NP559745.RAMCmcRddl0eUl9rMjJXcInOrhh-hHLo3iBdzm-clC6TE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:37+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" .
}