@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP240643.RAYa1RPAMufmNrcg1Yt-J18q_zjI7uxk2R6lyh8r57oFw
> .
@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:NP240643.RAYa1RPAMufmNrcg1Yt-J18q_zjI7uxk2R6lyh8r57oFw130_head
{
this:
np:hasAssertion
dgn-np:NP240643.RAYa1RPAMufmNrcg1Yt-J18q_zjI7uxk2R6lyh8r57oFw130_assertion
;
np:hasProvenance
dgn-np:NP240643.RAYa1RPAMufmNrcg1Yt-J18q_zjI7uxk2R6lyh8r57oFw130_provenance
;
np:hasPublicationInfo
dgn-np:NP240643.RAYa1RPAMufmNrcg1Yt-J18q_zjI7uxk2R6lyh8r57oFw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP240643.RAYa1RPAMufmNrcg1Yt-J18q_zjI7uxk2R6lyh8r57oFw130_assertion
a
np:Assertion
.
dgn-np:NP240643.RAYa1RPAMufmNrcg1Yt-J18q_zjI7uxk2R6lyh8r57oFw130_provenance
a
np:Provenance
.
dgn-np:NP240643.RAYa1RPAMufmNrcg1Yt-J18q_zjI7uxk2R6lyh8r57oFw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP240643.RAYa1RPAMufmNrcg1Yt-J18q_zjI7uxk2R6lyh8r57oFw130_assertion
{
miriam-gene:2525
a
ncit:C16612
.
lld:C0027126
a
ncit:C7057
.
dgn-gda:DGN91cde1cd5c2ad8a039fcb87cef1c0cec
sio:SIO_000628
miriam-gene:2525
,
lld:C0027126
;
a
sio:SIO_001121
.
}
dgn-np:NP240643.RAYa1RPAMufmNrcg1Yt-J18q_zjI7uxk2R6lyh8r57oFw130_provenance
{
dgn-np:NP240643.RAYa1RPAMufmNrcg1Yt-J18q_zjI7uxk2R6lyh8r57oFw130_assertion
dcterms:description
"[As to linkage relationships of C3 with marker systems and with myotonic dystrophy, there was evidence (most of it first presented at the 6th International Congress of Human Genetics, Jerusalem 1981) for synteny with ABH secretion (Se): C3-Se (males) z = 4.35, theta = 0.12 and with Lewis secretion (LES): C3-LES (males z = 3.63, theta = 0.04).]. 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:6627719
;
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:NP240643.RAYa1RPAMufmNrcg1Yt-J18q_zjI7uxk2R6lyh8r57oFw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}