Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP921549.RAuv8J0H0Z8ToLmAtSA87NV1dhQ_HL7U4syJq_TOt2dKA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP921549.RAuv8J0H0Z8ToLmAtSA87NV1dhQ_HL7U4syJq_TOt2dKA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP921549.RAuv8J0H0Z8ToLmAtSA87NV1dhQ_HL7U4syJq_TOt2dKA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP921549.RAuv8J0H0Z8ToLmAtSA87NV1dhQ_HL7U4syJq_TOt2dKA130_provenance.
- NP921549.RAuv8J0H0Z8ToLmAtSA87NV1dhQ_HL7U4syJq_TOt2dKA130_assertion description "[Novel V97G ASAH1 mutation found in Farber disease patients: unique appearance of the disease with an intermediate severity, and marked early involvement of central and peripheral nervous system.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP921549.RAuv8J0H0Z8ToLmAtSA87NV1dhQ_HL7U4syJq_TOt2dKA130_provenance.
- NP921549.RAuv8J0H0Z8ToLmAtSA87NV1dhQ_HL7U4syJq_TOt2dKA130_assertion evidence source_evidence_literature NP921549.RAuv8J0H0Z8ToLmAtSA87NV1dhQ_HL7U4syJq_TOt2dKA130_provenance.
- NP921549.RAuv8J0H0Z8ToLmAtSA87NV1dhQ_HL7U4syJq_TOt2dKA130_assertion SIO_000772 21893389 NP921549.RAuv8J0H0Z8ToLmAtSA87NV1dhQ_HL7U4syJq_TOt2dKA130_provenance.
- NP921549.RAuv8J0H0Z8ToLmAtSA87NV1dhQ_HL7U4syJq_TOt2dKA130_assertion wasDerivedFrom befree-2016 NP921549.RAuv8J0H0Z8ToLmAtSA87NV1dhQ_HL7U4syJq_TOt2dKA130_provenance.
- NP921549.RAuv8J0H0Z8ToLmAtSA87NV1dhQ_HL7U4syJq_TOt2dKA130_assertion wasGeneratedBy ECO_0000203 NP921549.RAuv8J0H0Z8ToLmAtSA87NV1dhQ_HL7U4syJq_TOt2dKA130_provenance.
- befree-2016 importedOn "2016-02-19" NP921549.RAuv8J0H0Z8ToLmAtSA87NV1dhQ_HL7U4syJq_TOt2dKA130_provenance.