@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ
> .
@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:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_head
{
this:
np:hasAssertion
dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_assertion
;
np:hasProvenance
dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_assertion
a
np:Assertion
.
dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_provenance
a
np:Provenance
.
dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_assertion
{
miriam-gene:2064
a
ncit:C16612
.
lld:C0030186
a
ncit:C7057
.
dgn-gda:DGNff236fe6e4ed69d74d0decc2570fd22e
sio:SIO_000628
miriam-gene:2064
,
lld:C0030186
;
a
sio:SIO_001121
.
}
dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_provenance
{
dgn-np:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_assertion
dcterms:description
"[These results suggest the contribution of the HER2 signaling pathway to the pathogenesis and progression of some cases of extramammary Paget's disease, for which clinical use of molecular target therapy against the HER2 pathway is warranted.]. 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:16311120
;
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:NP317264.RAczCGkBpy9HmvfvcwbmbBPSxov2Uc1W8Fsp84jnWKqMQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:04+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" .
}