Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP802719.RAA-NI-KplUatQP3V3mB2Y_UEPHFFEcd49O0xAVFqNurY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP802719.RAA-NI-KplUatQP3V3mB2Y_UEPHFFEcd49O0xAVFqNurY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP802719.RAA-NI-KplUatQP3V3mB2Y_UEPHFFEcd49O0xAVFqNurY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP802719.RAA-NI-KplUatQP3V3mB2Y_UEPHFFEcd49O0xAVFqNurY130_provenance.
- NP802719.RAA-NI-KplUatQP3V3mB2Y_UEPHFFEcd49O0xAVFqNurY130_assertion description "[In order to obtain insight into the aetiology and pathogenesis of amyotrophic lateral sclerosis (ALS), high-density gene discovery arrays (GDA human version 1.2) containing 18 400 non-redundant EST cDNAs pooled from different tissue libraries have been used to monitor gene expression in lumbar spinal cord from ALS cases compared with controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP802719.RAA-NI-KplUatQP3V3mB2Y_UEPHFFEcd49O0xAVFqNurY130_provenance.
- NP802719.RAA-NI-KplUatQP3V3mB2Y_UEPHFFEcd49O0xAVFqNurY130_assertion evidence source_evidence_literature NP802719.RAA-NI-KplUatQP3V3mB2Y_UEPHFFEcd49O0xAVFqNurY130_provenance.
- NP802719.RAA-NI-KplUatQP3V3mB2Y_UEPHFFEcd49O0xAVFqNurY130_assertion SIO_000772 11279269 NP802719.RAA-NI-KplUatQP3V3mB2Y_UEPHFFEcd49O0xAVFqNurY130_provenance.
- NP802719.RAA-NI-KplUatQP3V3mB2Y_UEPHFFEcd49O0xAVFqNurY130_assertion wasDerivedFrom befree-20140225 NP802719.RAA-NI-KplUatQP3V3mB2Y_UEPHFFEcd49O0xAVFqNurY130_provenance.
- NP802719.RAA-NI-KplUatQP3V3mB2Y_UEPHFFEcd49O0xAVFqNurY130_assertion wasGeneratedBy ECO_0000203 NP802719.RAA-NI-KplUatQP3V3mB2Y_UEPHFFEcd49O0xAVFqNurY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP802719.RAA-NI-KplUatQP3V3mB2Y_UEPHFFEcd49O0xAVFqNurY130_provenance.