@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1380133.RAhBFtALIKpvaGMzOXFBQSIgDK3oEbxFg0wkS1j7461-U
> .
@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/v4.0.0/void/
> .
dgn-np:NP1380133.RAhBFtALIKpvaGMzOXFBQSIgDK3oEbxFg0wkS1j7461-U130_head
{
this:
np:hasAssertion
dgn-np:NP1380133.RAhBFtALIKpvaGMzOXFBQSIgDK3oEbxFg0wkS1j7461-U130_assertion
;
np:hasProvenance
dgn-np:NP1380133.RAhBFtALIKpvaGMzOXFBQSIgDK3oEbxFg0wkS1j7461-U130_provenance
;
np:hasPublicationInfo
dgn-np:NP1380133.RAhBFtALIKpvaGMzOXFBQSIgDK3oEbxFg0wkS1j7461-U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1380133.RAhBFtALIKpvaGMzOXFBQSIgDK3oEbxFg0wkS1j7461-U130_assertion
a
np:Assertion
.
dgn-np:NP1380133.RAhBFtALIKpvaGMzOXFBQSIgDK3oEbxFg0wkS1j7461-U130_provenance
a
np:Provenance
.
dgn-np:NP1380133.RAhBFtALIKpvaGMzOXFBQSIgDK3oEbxFg0wkS1j7461-U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1380133.RAhBFtALIKpvaGMzOXFBQSIgDK3oEbxFg0wkS1j7461-U130_assertion
{
miriam-gene:4436
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGNe2273b6d00e07668c6f1d3f0229e41fc
sio:SIO_000628
miriam-gene:4436
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP1380133.RAhBFtALIKpvaGMzOXFBQSIgDK3oEbxFg0wkS1j7461-U130_provenance
{
dgn-np:NP1380133.RAhBFtALIKpvaGMzOXFBQSIgDK3oEbxFg0wkS1j7461-U130_assertion
dcterms:description
"[These results provide a clarification of the contribution of hMSH2 and hMLH1 to the HNPCC phenotype and suggest that in the majority of Eastern United States HNPCC kindreds selected by phenotype alone, the molecular genetic basis for the disease remains unknown.]. 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:9288790
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1380133.RAhBFtALIKpvaGMzOXFBQSIgDK3oEbxFg0wkS1j7461-U130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:11+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}