Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP427437.RAY_YZlq2ZxMYml0RyLhy5GtJ3089V69bCYO5CfD1NpTk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP427437.RAY_YZlq2ZxMYml0RyLhy5GtJ3089V69bCYO5CfD1NpTk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP427437.RAY_YZlq2ZxMYml0RyLhy5GtJ3089V69bCYO5CfD1NpTk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP427437.RAY_YZlq2ZxMYml0RyLhy5GtJ3089V69bCYO5CfD1NpTk130_provenance.
- NP427437.RAY_YZlq2ZxMYml0RyLhy5GtJ3089V69bCYO5CfD1NpTk130_assertion description "[In many of autosomal dominant diseases such as familial amyotrophic lateral sclerosis (ALS) with SOD1 mutation, a missense point mutation may induce the disease by its gain of adverse property.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP427437.RAY_YZlq2ZxMYml0RyLhy5GtJ3089V69bCYO5CfD1NpTk130_provenance.
- NP427437.RAY_YZlq2ZxMYml0RyLhy5GtJ3089V69bCYO5CfD1NpTk130_assertion evidence source_evidence_literature NP427437.RAY_YZlq2ZxMYml0RyLhy5GtJ3089V69bCYO5CfD1NpTk130_provenance.
- NP427437.RAY_YZlq2ZxMYml0RyLhy5GtJ3089V69bCYO5CfD1NpTk130_assertion SIO_000772 14715277 NP427437.RAY_YZlq2ZxMYml0RyLhy5GtJ3089V69bCYO5CfD1NpTk130_provenance.
- NP427437.RAY_YZlq2ZxMYml0RyLhy5GtJ3089V69bCYO5CfD1NpTk130_assertion wasDerivedFrom befree-2016 NP427437.RAY_YZlq2ZxMYml0RyLhy5GtJ3089V69bCYO5CfD1NpTk130_provenance.
- NP427437.RAY_YZlq2ZxMYml0RyLhy5GtJ3089V69bCYO5CfD1NpTk130_assertion wasGeneratedBy ECO_0000203 NP427437.RAY_YZlq2ZxMYml0RyLhy5GtJ3089V69bCYO5CfD1NpTk130_provenance.
- befree-2016 importedOn "2016-02-19" NP427437.RAY_YZlq2ZxMYml0RyLhy5GtJ3089V69bCYO5CfD1NpTk130_provenance.