@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP192070.RAhC_w5GiEEF6s2nL4OJ6DuvG5-OtJsU9ih26u2bcIuG0
> .
@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:NP192070.RAhC_w5GiEEF6s2nL4OJ6DuvG5-OtJsU9ih26u2bcIuG0130_head
{
this:
np:hasAssertion
dgn-np:NP192070.RAhC_w5GiEEF6s2nL4OJ6DuvG5-OtJsU9ih26u2bcIuG0130_assertion
;
np:hasProvenance
dgn-np:NP192070.RAhC_w5GiEEF6s2nL4OJ6DuvG5-OtJsU9ih26u2bcIuG0130_provenance
;
np:hasPublicationInfo
dgn-np:NP192070.RAhC_w5GiEEF6s2nL4OJ6DuvG5-OtJsU9ih26u2bcIuG0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP192070.RAhC_w5GiEEF6s2nL4OJ6DuvG5-OtJsU9ih26u2bcIuG0130_assertion
a
np:Assertion
.
dgn-np:NP192070.RAhC_w5GiEEF6s2nL4OJ6DuvG5-OtJsU9ih26u2bcIuG0130_provenance
a
np:Provenance
.
dgn-np:NP192070.RAhC_w5GiEEF6s2nL4OJ6DuvG5-OtJsU9ih26u2bcIuG0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP192070.RAhC_w5GiEEF6s2nL4OJ6DuvG5-OtJsU9ih26u2bcIuG0130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN135d6c2e0737db8b590fdf3a68734edc
sio:SIO_000628
miriam-gene:4360
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP192070.RAhC_w5GiEEF6s2nL4OJ6DuvG5-OtJsU9ih26u2bcIuG0130_provenance
{
dgn-np:NP192070.RAhC_w5GiEEF6s2nL4OJ6DuvG5-OtJsU9ih26u2bcIuG0130_assertion
dcterms:description
"[Conversely, the high proportion of MSS tumors observed in our series of families with advanced age at cancer diagnosis is consistent with the low percentage of MMR mutations detected by previous studies in families with this phenotype.]. 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:15340262
;
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:NP192070.RAhC_w5GiEEF6s2nL4OJ6DuvG5-OtJsU9ih26u2bcIuG0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:45+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" .
}