@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP348244.RALYrfgAEIKVLgfVUl7D06jwHDFzuVUyregcuZqd5ZKbw130_head { this: np:hasAssertion dgn-np:NP348244.RALYrfgAEIKVLgfVUl7D06jwHDFzuVUyregcuZqd5ZKbw130_assertion; np:hasProvenance dgn-np:NP348244.RALYrfgAEIKVLgfVUl7D06jwHDFzuVUyregcuZqd5ZKbw130_provenance; np:hasPublicationInfo dgn-np:NP348244.RALYrfgAEIKVLgfVUl7D06jwHDFzuVUyregcuZqd5ZKbw130_publicationInfo; a np:Nanopublication . dgn-np:NP348244.RALYrfgAEIKVLgfVUl7D06jwHDFzuVUyregcuZqd5ZKbw130_assertion a np:Assertion . dgn-np:NP348244.RALYrfgAEIKVLgfVUl7D06jwHDFzuVUyregcuZqd5ZKbw130_provenance a np:Provenance . dgn-np:NP348244.RALYrfgAEIKVLgfVUl7D06jwHDFzuVUyregcuZqd5ZKbw130_publicationInfo a np:PublicationInfo . } dgn-np:NP348244.RALYrfgAEIKVLgfVUl7D06jwHDFzuVUyregcuZqd5ZKbw130_assertion { miriam-gene:1630 a ncit:C16612 . lld:C1527249 a ncit:C7057 . dgn-gda:DGNe4d753ad1dfd599ef53402fed4b13c05 sio:SIO_000628 miriam-gene:1630, lld:C1527249; a sio:SIO_001121 . } dgn-np:NP348244.RALYrfgAEIKVLgfVUl7D06jwHDFzuVUyregcuZqd5ZKbw130_provenance { dgn-np:NP348244.RALYrfgAEIKVLgfVUl7D06jwHDFzuVUyregcuZqd5ZKbw130_assertion dcterms:description "[Phenotypic analogy to mice with homozygous inactivation of Ntn1 encoding the secreted axonal guidance protein netrin1, or Dcc encoding its receptor Deleted in Colorectal Cancer led us to perform sequence analysis of NTN1 and DCC in all the patients.]. 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:17690130; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP348244.RALYrfgAEIKVLgfVUl7D06jwHDFzuVUyregcuZqd5ZKbw130_publicationInfo { this: dcterms:created "2015-08-25T14:41:00+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }