@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP543062.RAMj4pMFkXssQUN8j8OijGLAvoX8Yru0zGBNDmOgatzt0
> .
@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:NP543062.RAMj4pMFkXssQUN8j8OijGLAvoX8Yru0zGBNDmOgatzt0130_head
{
this:
np:hasAssertion
dgn-np:NP543062.RAMj4pMFkXssQUN8j8OijGLAvoX8Yru0zGBNDmOgatzt0130_assertion
;
np:hasProvenance
dgn-np:NP543062.RAMj4pMFkXssQUN8j8OijGLAvoX8Yru0zGBNDmOgatzt0130_provenance
;
np:hasPublicationInfo
dgn-np:NP543062.RAMj4pMFkXssQUN8j8OijGLAvoX8Yru0zGBNDmOgatzt0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP543062.RAMj4pMFkXssQUN8j8OijGLAvoX8Yru0zGBNDmOgatzt0130_assertion
a
np:Assertion
.
dgn-np:NP543062.RAMj4pMFkXssQUN8j8OijGLAvoX8Yru0zGBNDmOgatzt0130_provenance
a
np:Provenance
.
dgn-np:NP543062.RAMj4pMFkXssQUN8j8OijGLAvoX8Yru0zGBNDmOgatzt0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP543062.RAMj4pMFkXssQUN8j8OijGLAvoX8Yru0zGBNDmOgatzt0130_assertion
{
miriam-gene:11146
a
ncit:C16612
.
lld:C0699790
a
ncit:C7057
.
dgn-gda:DGN43fb9fdfd50097727891e7c0ea8b8eeb
sio:SIO_000628
miriam-gene:11146
,
lld:C0699790
;
a
sio:SIO_001121
.
}
dgn-np:NP543062.RAMj4pMFkXssQUN8j8OijGLAvoX8Yru0zGBNDmOgatzt0130_provenance
{
dgn-np:NP543062.RAMj4pMFkXssQUN8j8OijGLAvoX8Yru0zGBNDmOgatzt0130_assertion
dcterms:description
"[Involvement of the genes on 5q (FAP) and 18q (Lynch syndrome II) in hereditary colon cancer syndromes is supported by linkage studies, but their respective roles (as well as that of the gene on 17p) in familial and sporadic colorectal cancer remain to be precisely defined.]. 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:2645266
;
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:NP543062.RAMj4pMFkXssQUN8j8OijGLAvoX8Yru0zGBNDmOgatzt0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:27+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" .
}