Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1012562.RAJ_56QLcogtvikE6E0tGIsyOnHXtvgO2UPTwTodzPPAQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1012562.RAJ_56QLcogtvikE6E0tGIsyOnHXtvgO2UPTwTodzPPAQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1012562.RAJ_56QLcogtvikE6E0tGIsyOnHXtvgO2UPTwTodzPPAQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1012562.RAJ_56QLcogtvikE6E0tGIsyOnHXtvgO2UPTwTodzPPAQ130_provenance.
- NP1012562.RAJ_56QLcogtvikE6E0tGIsyOnHXtvgO2UPTwTodzPPAQ130_assertion description "[We identified 6 missense mutations in the coding region of SQSTM1 in patients with either FTLD or ALS, none of which were found in healthy controls or patients with PDB.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1012562.RAJ_56QLcogtvikE6E0tGIsyOnHXtvgO2UPTwTodzPPAQ130_provenance.
- NP1012562.RAJ_56QLcogtvikE6E0tGIsyOnHXtvgO2UPTwTodzPPAQ130_assertion evidence source_evidence_literature NP1012562.RAJ_56QLcogtvikE6E0tGIsyOnHXtvgO2UPTwTodzPPAQ130_provenance.
- NP1012562.RAJ_56QLcogtvikE6E0tGIsyOnHXtvgO2UPTwTodzPPAQ130_assertion SIO_000772 22972638 NP1012562.RAJ_56QLcogtvikE6E0tGIsyOnHXtvgO2UPTwTodzPPAQ130_provenance.
- NP1012562.RAJ_56QLcogtvikE6E0tGIsyOnHXtvgO2UPTwTodzPPAQ130_assertion wasDerivedFrom befree-2016 NP1012562.RAJ_56QLcogtvikE6E0tGIsyOnHXtvgO2UPTwTodzPPAQ130_provenance.
- NP1012562.RAJ_56QLcogtvikE6E0tGIsyOnHXtvgO2UPTwTodzPPAQ130_assertion wasGeneratedBy ECO_0000203 NP1012562.RAJ_56QLcogtvikE6E0tGIsyOnHXtvgO2UPTwTodzPPAQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1012562.RAJ_56QLcogtvikE6E0tGIsyOnHXtvgO2UPTwTodzPPAQ130_provenance.