@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP320898.RA8fK4RZjjO5KF5Jt5fqkwY-IjaiUx0gJUcKfTnmk_FP4
> .
@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:NP320898.RA8fK4RZjjO5KF5Jt5fqkwY-IjaiUx0gJUcKfTnmk_FP4130_head
{
this:
np:hasAssertion
dgn-np:NP320898.RA8fK4RZjjO5KF5Jt5fqkwY-IjaiUx0gJUcKfTnmk_FP4130_assertion
;
np:hasProvenance
dgn-np:NP320898.RA8fK4RZjjO5KF5Jt5fqkwY-IjaiUx0gJUcKfTnmk_FP4130_provenance
;
np:hasPublicationInfo
dgn-np:NP320898.RA8fK4RZjjO5KF5Jt5fqkwY-IjaiUx0gJUcKfTnmk_FP4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP320898.RA8fK4RZjjO5KF5Jt5fqkwY-IjaiUx0gJUcKfTnmk_FP4130_assertion
a
np:Assertion
.
dgn-np:NP320898.RA8fK4RZjjO5KF5Jt5fqkwY-IjaiUx0gJUcKfTnmk_FP4130_provenance
a
np:Provenance
.
dgn-np:NP320898.RA8fK4RZjjO5KF5Jt5fqkwY-IjaiUx0gJUcKfTnmk_FP4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP320898.RA8fK4RZjjO5KF5Jt5fqkwY-IjaiUx0gJUcKfTnmk_FP4130_assertion
{
miriam-gene:79577
a
ncit:C16612
.
lld:C0027662
a
ncit:C7057
.
dgn-gda:DGN8c4e6a434a60c4dcff50a0ac3ae7311c
sio:SIO_000628
miriam-gene:79577
,
lld:C0027662
;
a
sio:SIO_001121
.
}
dgn-np:NP320898.RA8fK4RZjjO5KF5Jt5fqkwY-IjaiUx0gJUcKfTnmk_FP4130_provenance
{
dgn-np:NP320898.RA8fK4RZjjO5KF5Jt5fqkwY-IjaiUx0gJUcKfTnmk_FP4130_assertion
dcterms:description
"[Studies in DNA linkage were performed within this large family and a similar family in Houston to determine if the gene for this syndrome, termed HRPT2, is linked to DNA markers on chromosome 11, to which the gene for multiple endocrine neoplasia (MEN) type 1 has been linked.]. 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:2123361
;
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:NP320898.RA8fK4RZjjO5KF5Jt5fqkwY-IjaiUx0gJUcKfTnmk_FP4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:06+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" .
}