Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1267869.RA7dk8vJdSMTuWiuoTpQvmf_6BEF0pcs9sOy9N23z2U4k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1267869.RA7dk8vJdSMTuWiuoTpQvmf_6BEF0pcs9sOy9N23z2U4k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1267869.RA7dk8vJdSMTuWiuoTpQvmf_6BEF0pcs9sOy9N23z2U4k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1267869.RA7dk8vJdSMTuWiuoTpQvmf_6BEF0pcs9sOy9N23z2U4k130_provenance.
- NP1267869.RA7dk8vJdSMTuWiuoTpQvmf_6BEF0pcs9sOy9N23z2U4k130_assertion description "[Our observations linking U1 snRNP to ALS patient cells with FUS mutations, SMN-containing Gems, and motor neurons indicate that U1 snRNP is a component of a molecular pathway associated with motor neuron disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1267869.RA7dk8vJdSMTuWiuoTpQvmf_6BEF0pcs9sOy9N23z2U4k130_provenance.
- NP1267869.RA7dk8vJdSMTuWiuoTpQvmf_6BEF0pcs9sOy9N23z2U4k130_assertion evidence source_evidence_literature NP1267869.RA7dk8vJdSMTuWiuoTpQvmf_6BEF0pcs9sOy9N23z2U4k130_provenance.
- NP1267869.RA7dk8vJdSMTuWiuoTpQvmf_6BEF0pcs9sOy9N23z2U4k130_assertion SIO_000772 25735748 NP1267869.RA7dk8vJdSMTuWiuoTpQvmf_6BEF0pcs9sOy9N23z2U4k130_provenance.
- NP1267869.RA7dk8vJdSMTuWiuoTpQvmf_6BEF0pcs9sOy9N23z2U4k130_assertion wasDerivedFrom befree-2016 NP1267869.RA7dk8vJdSMTuWiuoTpQvmf_6BEF0pcs9sOy9N23z2U4k130_provenance.
- NP1267869.RA7dk8vJdSMTuWiuoTpQvmf_6BEF0pcs9sOy9N23z2U4k130_assertion wasGeneratedBy ECO_0000203 NP1267869.RA7dk8vJdSMTuWiuoTpQvmf_6BEF0pcs9sOy9N23z2U4k130_provenance.
- befree-2016 importedOn "2016-02-19" NP1267869.RA7dk8vJdSMTuWiuoTpQvmf_6BEF0pcs9sOy9N23z2U4k130_provenance.