@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP544194.RAmIyDC4lJ70QerrIRL8Q-WJmkNHVF2sGPxvvcRkrLOqk
> .
@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:NP544194.RAmIyDC4lJ70QerrIRL8Q-WJmkNHVF2sGPxvvcRkrLOqk130_head
{
this:
np:hasAssertion
dgn-np:NP544194.RAmIyDC4lJ70QerrIRL8Q-WJmkNHVF2sGPxvvcRkrLOqk130_assertion
;
np:hasProvenance
dgn-np:NP544194.RAmIyDC4lJ70QerrIRL8Q-WJmkNHVF2sGPxvvcRkrLOqk130_provenance
;
np:hasPublicationInfo
dgn-np:NP544194.RAmIyDC4lJ70QerrIRL8Q-WJmkNHVF2sGPxvvcRkrLOqk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP544194.RAmIyDC4lJ70QerrIRL8Q-WJmkNHVF2sGPxvvcRkrLOqk130_assertion
a
np:Assertion
.
dgn-np:NP544194.RAmIyDC4lJ70QerrIRL8Q-WJmkNHVF2sGPxvvcRkrLOqk130_provenance
a
np:Provenance
.
dgn-np:NP544194.RAmIyDC4lJ70QerrIRL8Q-WJmkNHVF2sGPxvvcRkrLOqk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP544194.RAmIyDC4lJ70QerrIRL8Q-WJmkNHVF2sGPxvvcRkrLOqk130_assertion
{
miriam-gene:5378
a
ncit:C16612
.
lld:C0007102
a
ncit:C7057
.
dgn-gda:DGN4c0d348aa27d7f01cfa6c81cdc5991ea
sio:SIO_000628
miriam-gene:5378
,
lld:C0007102
;
a
sio:SIO_001121
.
}
dgn-np:NP544194.RAmIyDC4lJ70QerrIRL8Q-WJmkNHVF2sGPxvvcRkrLOqk130_provenance
{
dgn-np:NP544194.RAmIyDC4lJ70QerrIRL8Q-WJmkNHVF2sGPxvvcRkrLOqk130_assertion
dcterms:description
"[Functional redundancy among Mlh3, Pms1 and Pms2 may explain why neither Pms1 nor Pms2 mutant mice develop colon cancer, and why PMS1 and PMS2 mutations are only rarely found in HNPCC families.]. 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:10615123
;
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:NP544194.RAmIyDC4lJ70QerrIRL8Q-WJmkNHVF2sGPxvvcRkrLOqk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:28+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" .
}