Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP307809.RAE2AeN3gQwLj9PwdEtRZnwkSI3CRLJE525Ou2-oYMc-o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP307809.RAE2AeN3gQwLj9PwdEtRZnwkSI3CRLJE525Ou2-oYMc-o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP307809.RAE2AeN3gQwLj9PwdEtRZnwkSI3CRLJE525Ou2-oYMc-o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP307809.RAE2AeN3gQwLj9PwdEtRZnwkSI3CRLJE525Ou2-oYMc-o130_provenance.
- NP307809.RAE2AeN3gQwLj9PwdEtRZnwkSI3CRLJE525Ou2-oYMc-o130_assertion description "[Hereditary frontotemporal dementia with Parkinsonism linked to chromosome 17 (FTDP-17) is associated with different mutations in the microtubule-associated protein (MAP) tau gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP307809.RAE2AeN3gQwLj9PwdEtRZnwkSI3CRLJE525Ou2-oYMc-o130_provenance.
- NP307809.RAE2AeN3gQwLj9PwdEtRZnwkSI3CRLJE525Ou2-oYMc-o130_assertion evidence source_evidence_literature NP307809.RAE2AeN3gQwLj9PwdEtRZnwkSI3CRLJE525Ou2-oYMc-o130_provenance.
- NP307809.RAE2AeN3gQwLj9PwdEtRZnwkSI3CRLJE525Ou2-oYMc-o130_assertion SIO_000772 11193139 NP307809.RAE2AeN3gQwLj9PwdEtRZnwkSI3CRLJE525Ou2-oYMc-o130_provenance.
- NP307809.RAE2AeN3gQwLj9PwdEtRZnwkSI3CRLJE525Ou2-oYMc-o130_assertion wasDerivedFrom befree-2016 NP307809.RAE2AeN3gQwLj9PwdEtRZnwkSI3CRLJE525Ou2-oYMc-o130_provenance.
- NP307809.RAE2AeN3gQwLj9PwdEtRZnwkSI3CRLJE525Ou2-oYMc-o130_assertion wasGeneratedBy ECO_0000203 NP307809.RAE2AeN3gQwLj9PwdEtRZnwkSI3CRLJE525Ou2-oYMc-o130_provenance.
- befree-2016 importedOn "2016-02-19" NP307809.RAE2AeN3gQwLj9PwdEtRZnwkSI3CRLJE525Ou2-oYMc-o130_provenance.