@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP678457.RAi1EB7R1OcOQEmDIlgRenvMp_yCr-dXjHfIVvHTaWGdY
> .
@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:NP678457.RAi1EB7R1OcOQEmDIlgRenvMp_yCr-dXjHfIVvHTaWGdY130_head
{
this:
np:hasAssertion
dgn-np:NP678457.RAi1EB7R1OcOQEmDIlgRenvMp_yCr-dXjHfIVvHTaWGdY130_assertion
;
np:hasProvenance
dgn-np:NP678457.RAi1EB7R1OcOQEmDIlgRenvMp_yCr-dXjHfIVvHTaWGdY130_provenance
;
np:hasPublicationInfo
dgn-np:NP678457.RAi1EB7R1OcOQEmDIlgRenvMp_yCr-dXjHfIVvHTaWGdY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP678457.RAi1EB7R1OcOQEmDIlgRenvMp_yCr-dXjHfIVvHTaWGdY130_assertion
a
np:Assertion
.
dgn-np:NP678457.RAi1EB7R1OcOQEmDIlgRenvMp_yCr-dXjHfIVvHTaWGdY130_provenance
a
np:Provenance
.
dgn-np:NP678457.RAi1EB7R1OcOQEmDIlgRenvMp_yCr-dXjHfIVvHTaWGdY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP678457.RAi1EB7R1OcOQEmDIlgRenvMp_yCr-dXjHfIVvHTaWGdY130_assertion
{
miriam-gene:1719
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGNbaa5951af3e3f5eb62ab64cefc7f4b01
sio:SIO_000628
miriam-gene:1719
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP678457.RAi1EB7R1OcOQEmDIlgRenvMp_yCr-dXjHfIVvHTaWGdY130_provenance
{
dgn-np:NP678457.RAi1EB7R1OcOQEmDIlgRenvMp_yCr-dXjHfIVvHTaWGdY130_assertion
dcterms:description
"[Further analyses of DHFR, MLL, MYC, and RFC gene status in four additional human OS cell lines revealed that only gain of DHFR and MLL were associated with an inherent lower sensitivity to MTX.]. 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:14582536
;
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:NP678457.RAi1EB7R1OcOQEmDIlgRenvMp_yCr-dXjHfIVvHTaWGdY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:49+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" .
}