Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP972755.RAgpW8aulC3mcs9cYHWcoJmy6gCyhp2mdEXW5LgP_jhvI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP972755.RAgpW8aulC3mcs9cYHWcoJmy6gCyhp2mdEXW5LgP_jhvI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP972755.RAgpW8aulC3mcs9cYHWcoJmy6gCyhp2mdEXW5LgP_jhvI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP972755.RAgpW8aulC3mcs9cYHWcoJmy6gCyhp2mdEXW5LgP_jhvI130_provenance.
- NP972755.RAgpW8aulC3mcs9cYHWcoJmy6gCyhp2mdEXW5LgP_jhvI130_assertion description "[A number of autosomal-dominant genes have been described that primarily cause ALS or FTLD such as progranulin (GRN), valosin-containing protein (VCP), and TAR DNA-Binding Protein (TARDBP), and for each of these conditions there are a small number of cases with both ALS and FTLD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP972755.RAgpW8aulC3mcs9cYHWcoJmy6gCyhp2mdEXW5LgP_jhvI130_provenance.
- NP972755.RAgpW8aulC3mcs9cYHWcoJmy6gCyhp2mdEXW5LgP_jhvI130_assertion evidence source_evidence_literature NP972755.RAgpW8aulC3mcs9cYHWcoJmy6gCyhp2mdEXW5LgP_jhvI130_provenance.
- NP972755.RAgpW8aulC3mcs9cYHWcoJmy6gCyhp2mdEXW5LgP_jhvI130_assertion SIO_000772 22477152 NP972755.RAgpW8aulC3mcs9cYHWcoJmy6gCyhp2mdEXW5LgP_jhvI130_provenance.
- NP972755.RAgpW8aulC3mcs9cYHWcoJmy6gCyhp2mdEXW5LgP_jhvI130_assertion wasDerivedFrom befree-2016 NP972755.RAgpW8aulC3mcs9cYHWcoJmy6gCyhp2mdEXW5LgP_jhvI130_provenance.
- NP972755.RAgpW8aulC3mcs9cYHWcoJmy6gCyhp2mdEXW5LgP_jhvI130_assertion wasGeneratedBy ECO_0000203 NP972755.RAgpW8aulC3mcs9cYHWcoJmy6gCyhp2mdEXW5LgP_jhvI130_provenance.
- befree-2016 importedOn "2016-02-19" NP972755.RAgpW8aulC3mcs9cYHWcoJmy6gCyhp2mdEXW5LgP_jhvI130_provenance.