@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP774168.RAnSVfgnvUSRWLsoNx8GlU5Agl1gKmoY9wYCXHAvB67kw
> .
@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:NP774168.RAnSVfgnvUSRWLsoNx8GlU5Agl1gKmoY9wYCXHAvB67kw130_head
{
this:
np:hasAssertion
dgn-np:NP774168.RAnSVfgnvUSRWLsoNx8GlU5Agl1gKmoY9wYCXHAvB67kw130_assertion
;
np:hasProvenance
dgn-np:NP774168.RAnSVfgnvUSRWLsoNx8GlU5Agl1gKmoY9wYCXHAvB67kw130_provenance
;
np:hasPublicationInfo
dgn-np:NP774168.RAnSVfgnvUSRWLsoNx8GlU5Agl1gKmoY9wYCXHAvB67kw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP774168.RAnSVfgnvUSRWLsoNx8GlU5Agl1gKmoY9wYCXHAvB67kw130_assertion
a
np:Assertion
.
dgn-np:NP774168.RAnSVfgnvUSRWLsoNx8GlU5Agl1gKmoY9wYCXHAvB67kw130_provenance
a
np:Provenance
.
dgn-np:NP774168.RAnSVfgnvUSRWLsoNx8GlU5Agl1gKmoY9wYCXHAvB67kw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP774168.RAnSVfgnvUSRWLsoNx8GlU5Agl1gKmoY9wYCXHAvB67kw130_assertion
{
miriam-gene:869
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN0b4ab0bf73befa243d548e38b4e7ce4f
sio:SIO_000628
miriam-gene:869
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP774168.RAnSVfgnvUSRWLsoNx8GlU5Agl1gKmoY9wYCXHAvB67kw130_provenance
{
dgn-np:NP774168.RAnSVfgnvUSRWLsoNx8GlU5Agl1gKmoY9wYCXHAvB67kw130_assertion
dcterms:description
"[Nonetheless, to realize the full potential of personalized care using RLHC requires advances in CER and biostatistics methodology and the development of interoperable informatics systems, which has been recognized by the National Cancer Institute's program for CER and personalized medicine.]. 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:23071236
;
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:NP774168.RAnSVfgnvUSRWLsoNx8GlU5Agl1gKmoY9wYCXHAvB67kw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:48+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" .
}