Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP376186.RAOQ4tT860Kvk1eMOvRO-W-ViztbBnskmcaKUs4ulrfUM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP376186.RAOQ4tT860Kvk1eMOvRO-W-ViztbBnskmcaKUs4ulrfUM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP376186.RAOQ4tT860Kvk1eMOvRO-W-ViztbBnskmcaKUs4ulrfUM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP376186.RAOQ4tT860Kvk1eMOvRO-W-ViztbBnskmcaKUs4ulrfUM130_provenance.
- befree-2016 importedOn "2016-02-19" NP376186.RAOQ4tT860Kvk1eMOvRO-W-ViztbBnskmcaKUs4ulrfUM130_provenance.
- NP376186.RAOQ4tT860Kvk1eMOvRO-W-ViztbBnskmcaKUs4ulrfUM130_assertion wasGeneratedBy ECO_0000203 NP376186.RAOQ4tT860Kvk1eMOvRO-W-ViztbBnskmcaKUs4ulrfUM130_provenance.
- NP376186.RAOQ4tT860Kvk1eMOvRO-W-ViztbBnskmcaKUs4ulrfUM130_assertion wasDerivedFrom befree-2016 NP376186.RAOQ4tT860Kvk1eMOvRO-W-ViztbBnskmcaKUs4ulrfUM130_provenance.
- NP376186.RAOQ4tT860Kvk1eMOvRO-W-ViztbBnskmcaKUs4ulrfUM130_assertion SIO_000772 12459588 NP376186.RAOQ4tT860Kvk1eMOvRO-W-ViztbBnskmcaKUs4ulrfUM130_provenance.
- NP376186.RAOQ4tT860Kvk1eMOvRO-W-ViztbBnskmcaKUs4ulrfUM130_assertion evidence source_evidence_literature NP376186.RAOQ4tT860Kvk1eMOvRO-W-ViztbBnskmcaKUs4ulrfUM130_provenance.
- NP376186.RAOQ4tT860Kvk1eMOvRO-W-ViztbBnskmcaKUs4ulrfUM130_assertion description "[Truncating neurotrypsin mutation in autosomal recessive nonsyndromic mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP376186.RAOQ4tT860Kvk1eMOvRO-W-ViztbBnskmcaKUs4ulrfUM130_provenance.