@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP503462.RAhOWaIqE0ZkCAgdudFgSsjYi1sxR0CPVo-l85Vkj1bL4
> .
@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:NP503462.RAhOWaIqE0ZkCAgdudFgSsjYi1sxR0CPVo-l85Vkj1bL4130_head
{
this:
np:hasAssertion
dgn-np:NP503462.RAhOWaIqE0ZkCAgdudFgSsjYi1sxR0CPVo-l85Vkj1bL4130_assertion
;
np:hasProvenance
dgn-np:NP503462.RAhOWaIqE0ZkCAgdudFgSsjYi1sxR0CPVo-l85Vkj1bL4130_provenance
;
np:hasPublicationInfo
dgn-np:NP503462.RAhOWaIqE0ZkCAgdudFgSsjYi1sxR0CPVo-l85Vkj1bL4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP503462.RAhOWaIqE0ZkCAgdudFgSsjYi1sxR0CPVo-l85Vkj1bL4130_assertion
a
np:Assertion
.
dgn-np:NP503462.RAhOWaIqE0ZkCAgdudFgSsjYi1sxR0CPVo-l85Vkj1bL4130_provenance
a
np:Provenance
.
dgn-np:NP503462.RAhOWaIqE0ZkCAgdudFgSsjYi1sxR0CPVo-l85Vkj1bL4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP503462.RAhOWaIqE0ZkCAgdudFgSsjYi1sxR0CPVo-l85Vkj1bL4130_assertion
{
miriam-gene:2272
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGNf42b0564de80a74c202be6a4b7180999
sio:SIO_000628
miriam-gene:2272
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP503462.RAhOWaIqE0ZkCAgdudFgSsjYi1sxR0CPVo-l85Vkj1bL4130_provenance
{
dgn-np:NP503462.RAhOWaIqE0ZkCAgdudFgSsjYi1sxR0CPVo-l85Vkj1bL4130_assertion
dcterms:description
"[These results support the hypothesis that deficiency in a MMR gene could be a cause of the high frequency of alterations in Fhit expression, and they permit the suggestion that FHIT gene alteration may be part of the genetic pathway involving MSI through which some colorectal cancers arise.]. 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:15196543
;
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:NP503462.RAhOWaIqE0ZkCAgdudFgSsjYi1sxR0CPVo-l85Vkj1bL4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:00+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" .
}