@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP305833.RAllQdi_U_U6Sh038L5swI2aDZ4ihvddGYUbVd4wrevAQ
> .
@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:NP305833.RAllQdi_U_U6Sh038L5swI2aDZ4ihvddGYUbVd4wrevAQ130_head
{
this:
np:hasAssertion
dgn-np:NP305833.RAllQdi_U_U6Sh038L5swI2aDZ4ihvddGYUbVd4wrevAQ130_assertion
;
np:hasProvenance
dgn-np:NP305833.RAllQdi_U_U6Sh038L5swI2aDZ4ihvddGYUbVd4wrevAQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP305833.RAllQdi_U_U6Sh038L5swI2aDZ4ihvddGYUbVd4wrevAQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP305833.RAllQdi_U_U6Sh038L5swI2aDZ4ihvddGYUbVd4wrevAQ130_assertion
a
np:Assertion
.
dgn-np:NP305833.RAllQdi_U_U6Sh038L5swI2aDZ4ihvddGYUbVd4wrevAQ130_provenance
a
np:Provenance
.
dgn-np:NP305833.RAllQdi_U_U6Sh038L5swI2aDZ4ihvddGYUbVd4wrevAQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP305833.RAllQdi_U_U6Sh038L5swI2aDZ4ihvddGYUbVd4wrevAQ130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C0376358
a
ncit:C7057
.
dgn-gda:DGN54fc8a4149be7281b466d0c78caf40ad
sio:SIO_000628
miriam-gene:4292
,
lld:C0376358
;
a
sio:SIO_001121
.
}
dgn-np:NP305833.RAllQdi_U_U6Sh038L5swI2aDZ4ihvddGYUbVd4wrevAQ130_provenance
{
dgn-np:NP305833.RAllQdi_U_U6Sh038L5swI2aDZ4ihvddGYUbVd4wrevAQ130_assertion
dcterms:description
"[Second, the samples from Finnish hereditary prostate cancer (HPC) families were used for the screening of MLH1 mutations which produced twelve MLH1 sequence variants including two missense mutations, I219V, as in the PRCA-colon cancer patient, and V647M.]. 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:16963262
;
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:NP305833.RAllQdi_U_U6Sh038L5swI2aDZ4ihvddGYUbVd4wrevAQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:55+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" .
}