@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP373922.RAP7A0-LdwK_r-9QzlAja-xb92SgtbL40AcIv1hSnmSLY
> .
@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:NP373922.RAP7A0-LdwK_r-9QzlAja-xb92SgtbL40AcIv1hSnmSLY130_head
{
this:
np:hasAssertion
dgn-np:NP373922.RAP7A0-LdwK_r-9QzlAja-xb92SgtbL40AcIv1hSnmSLY130_assertion
;
np:hasProvenance
dgn-np:NP373922.RAP7A0-LdwK_r-9QzlAja-xb92SgtbL40AcIv1hSnmSLY130_provenance
;
np:hasPublicationInfo
dgn-np:NP373922.RAP7A0-LdwK_r-9QzlAja-xb92SgtbL40AcIv1hSnmSLY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP373922.RAP7A0-LdwK_r-9QzlAja-xb92SgtbL40AcIv1hSnmSLY130_assertion
a
np:Assertion
.
dgn-np:NP373922.RAP7A0-LdwK_r-9QzlAja-xb92SgtbL40AcIv1hSnmSLY130_provenance
a
np:Provenance
.
dgn-np:NP373922.RAP7A0-LdwK_r-9QzlAja-xb92SgtbL40AcIv1hSnmSLY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP373922.RAP7A0-LdwK_r-9QzlAja-xb92SgtbL40AcIv1hSnmSLY130_assertion
{
miriam-gene:2064
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN0e26e21232226cda0a42224102865478
sio:SIO_000628
miriam-gene:2064
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP373922.RAP7A0-LdwK_r-9QzlAja-xb92SgtbL40AcIv1hSnmSLY130_provenance
{
dgn-np:NP373922.RAP7A0-LdwK_r-9QzlAja-xb92SgtbL40AcIv1hSnmSLY130_assertion
dcterms:description
"[The human epidermal growth factor Receptor 2 (HER2) seems to play an important role in the development of this neoplasia, and genetic alterations in this gene, such as point mutations and polymorphisms have been detected in breast cancer patients.]. 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:15167216
;
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:NP373922.RAP7A0-LdwK_r-9QzlAja-xb92SgtbL40AcIv1hSnmSLY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:39+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" .
}