@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP855187.RAoOjW-YNYpUhE-IE7A-KUOapZUKyexTHb_531NV-2w0w
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP855187.RAoOjW-YNYpUhE-IE7A-KUOapZUKyexTHb_531NV-2w0w130_assertion
;
np:hasProvenance
dgn-np:NP855187.RAoOjW-YNYpUhE-IE7A-KUOapZUKyexTHb_531NV-2w0w130_provenance
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np:hasPublicationInfo
dgn-np:NP855187.RAoOjW-YNYpUhE-IE7A-KUOapZUKyexTHb_531NV-2w0w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP855187.RAoOjW-YNYpUhE-IE7A-KUOapZUKyexTHb_531NV-2w0w130_assertion
a
np:Assertion
.
dgn-np:NP855187.RAoOjW-YNYpUhE-IE7A-KUOapZUKyexTHb_531NV-2w0w130_provenance
a
np:Provenance
.
dgn-np:NP855187.RAoOjW-YNYpUhE-IE7A-KUOapZUKyexTHb_531NV-2w0w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP855187.RAoOjW-YNYpUhE-IE7A-KUOapZUKyexTHb_531NV-2w0w130_assertion
{
miriam-gene:3621
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGNb24b65ee6582720e80981f49fe4e0bd1
sio:SIO_000628
miriam-gene:3621
,
lld:C0025202
;
a
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.
}
dgn-np:NP855187.RAoOjW-YNYpUhE-IE7A-KUOapZUKyexTHb_531NV-2w0w130_provenance
{
dgn-np:NP855187.RAoOjW-YNYpUhE-IE7A-KUOapZUKyexTHb_531NV-2w0w130_assertion
dcterms:description
"[To further investigate whether ING1 is involved in melanoma development, we examined the mutational status of the ING1 gene in 46 human cutaneous melanoma biopsies and characterized the biological importance of ING1 mutations in nucleotide excision repair.]. 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:15201991
;
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:NP855187.RAoOjW-YNYpUhE-IE7A-KUOapZUKyexTHb_531NV-2w0w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:43+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
<
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> , <
http://orcid.org/0000-0002-7534-7661
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> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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