@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP876101.RALCeahNX_DwZ3xzKwooJDEhjReOeOeVj52mop8D4JzjY
> .
@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:NP876101.RALCeahNX_DwZ3xzKwooJDEhjReOeOeVj52mop8D4JzjY130_head
{
this:
np:hasAssertion
dgn-np:NP876101.RALCeahNX_DwZ3xzKwooJDEhjReOeOeVj52mop8D4JzjY130_assertion
;
np:hasProvenance
dgn-np:NP876101.RALCeahNX_DwZ3xzKwooJDEhjReOeOeVj52mop8D4JzjY130_provenance
;
np:hasPublicationInfo
dgn-np:NP876101.RALCeahNX_DwZ3xzKwooJDEhjReOeOeVj52mop8D4JzjY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP876101.RALCeahNX_DwZ3xzKwooJDEhjReOeOeVj52mop8D4JzjY130_assertion
a
np:Assertion
.
dgn-np:NP876101.RALCeahNX_DwZ3xzKwooJDEhjReOeOeVj52mop8D4JzjY130_provenance
a
np:Provenance
.
dgn-np:NP876101.RALCeahNX_DwZ3xzKwooJDEhjReOeOeVj52mop8D4JzjY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP876101.RALCeahNX_DwZ3xzKwooJDEhjReOeOeVj52mop8D4JzjY130_assertion
{
miriam-gene:6573
a
ncit:C16612
.
lld:C0029463
a
ncit:C7057
.
dgn-gda:DGNcb7a1eb81037626221679b9165884766
sio:SIO_000628
miriam-gene:6573
,
lld:C0029463
;
a
sio:SIO_001121
.
}
dgn-np:NP876101.RALCeahNX_DwZ3xzKwooJDEhjReOeOeVj52mop8D4JzjY130_provenance
{
dgn-np:NP876101.RALCeahNX_DwZ3xzKwooJDEhjReOeOeVj52mop8D4JzjY130_assertion
dcterms:description
"[Whereas inactivating RFC mutations are a frequent mechanism of MTX resistance in human leukemia cell lines and in patients with osteosarcoma, they are not common and do not appear to play any significant role in intrinsic or acquired resistance to MTX in childhood leukemia.]. 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:14770434
;
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:NP876101.RALCeahNX_DwZ3xzKwooJDEhjReOeOeVj52mop8D4JzjY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:55+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" .
}