@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP166938.RAHukFMbS0Jv7OXs26VxQ3I1RLfE894GzAMyWKVcxNDDU
> .
@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:NP166938.RAHukFMbS0Jv7OXs26VxQ3I1RLfE894GzAMyWKVcxNDDU130_head
{
this:
np:hasAssertion
dgn-np:NP166938.RAHukFMbS0Jv7OXs26VxQ3I1RLfE894GzAMyWKVcxNDDU130_assertion
;
np:hasProvenance
dgn-np:NP166938.RAHukFMbS0Jv7OXs26VxQ3I1RLfE894GzAMyWKVcxNDDU130_provenance
;
np:hasPublicationInfo
dgn-np:NP166938.RAHukFMbS0Jv7OXs26VxQ3I1RLfE894GzAMyWKVcxNDDU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP166938.RAHukFMbS0Jv7OXs26VxQ3I1RLfE894GzAMyWKVcxNDDU130_assertion
a
np:Assertion
.
dgn-np:NP166938.RAHukFMbS0Jv7OXs26VxQ3I1RLfE894GzAMyWKVcxNDDU130_provenance
a
np:Provenance
.
dgn-np:NP166938.RAHukFMbS0Jv7OXs26VxQ3I1RLfE894GzAMyWKVcxNDDU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP166938.RAHukFMbS0Jv7OXs26VxQ3I1RLfE894GzAMyWKVcxNDDU130_assertion
{
miriam-gene:3207
a
ncit:C16612
.
lld:C0027962
a
ncit:C7057
.
dgn-gda:DGN355644423690fb57aa7b082f579801fd
sio:SIO_000628
miriam-gene:3207
,
lld:C0027962
;
a
sio:SIO_001121
.
}
dgn-np:NP166938.RAHukFMbS0Jv7OXs26VxQ3I1RLfE894GzAMyWKVcxNDDU130_provenance
{
dgn-np:NP166938.RAHukFMbS0Jv7OXs26VxQ3I1RLfE894GzAMyWKVcxNDDU130_assertion
dcterms:description
"[We found that the expression levels of HOXA11, A13, B9, D12 and D13 in melanoma were higher than those in nevus pigmentosus and that the expression levels of HOXA11, B2 and C13 were significantly different between pT4 melanoma and pT1 to pT3 melanoma.]. 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:15551325
;
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:NP166938.RAHukFMbS0Jv7OXs26VxQ3I1RLfE894GzAMyWKVcxNDDU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:30+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" .
}