@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_head
{
this:
np:hasAssertion
dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_assertion
;
np:hasProvenance
dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_provenance
;
np:hasPublicationInfo
dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_assertion
a
np:Assertion
.
dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_provenance
a
np:Provenance
.
dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C0153567
a
ncit:C7057
.
dgn-gda:DGNb9d956c4b413f77ba9b43d92e4421e31
sio:SIO_000628
miriam-gene:4292
,
lld:C0153567
;
a
sio:SIO_001122
.
}
dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_provenance
{
dgn-np:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_assertion
dcterms:description
"[The MLH1 D132H risk variant has significantly lower allele frequency in American compared with Israeli cancer patients and, alone, is unlikely to explain significant amounts of American sporadic colorectal cancer or uterine cancer susceptibility.]. 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:15991064
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP558306.RA0iYTfeEkl_suq1A_gwOA04wvn4wJbzKnSxbx7SWZRjM130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:12+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}