Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP570008.RA2sXcvDsWpLZ17BM_lMHTzmAHXOubbKwY17DXO3QxZ4E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP570008.RA2sXcvDsWpLZ17BM_lMHTzmAHXOubbKwY17DXO3QxZ4E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP570008.RA2sXcvDsWpLZ17BM_lMHTzmAHXOubbKwY17DXO3QxZ4E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP570008.RA2sXcvDsWpLZ17BM_lMHTzmAHXOubbKwY17DXO3QxZ4E130_provenance.
- NP570008.RA2sXcvDsWpLZ17BM_lMHTzmAHXOubbKwY17DXO3QxZ4E130_assertion description "[A previous study found significant linkage to chromosome 17 in a HDDD family (HDDD2), but no mutation in the MAPT gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570008.RA2sXcvDsWpLZ17BM_lMHTzmAHXOubbKwY17DXO3QxZ4E130_provenance.
- NP570008.RA2sXcvDsWpLZ17BM_lMHTzmAHXOubbKwY17DXO3QxZ4E130_assertion evidence source_evidence_literature NP570008.RA2sXcvDsWpLZ17BM_lMHTzmAHXOubbKwY17DXO3QxZ4E130_provenance.
- NP570008.RA2sXcvDsWpLZ17BM_lMHTzmAHXOubbKwY17DXO3QxZ4E130_assertion SIO_000772 16983685 NP570008.RA2sXcvDsWpLZ17BM_lMHTzmAHXOubbKwY17DXO3QxZ4E130_provenance.
- NP570008.RA2sXcvDsWpLZ17BM_lMHTzmAHXOubbKwY17DXO3QxZ4E130_assertion wasDerivedFrom befree-2016 NP570008.RA2sXcvDsWpLZ17BM_lMHTzmAHXOubbKwY17DXO3QxZ4E130_provenance.
- NP570008.RA2sXcvDsWpLZ17BM_lMHTzmAHXOubbKwY17DXO3QxZ4E130_assertion wasGeneratedBy ECO_0000203 NP570008.RA2sXcvDsWpLZ17BM_lMHTzmAHXOubbKwY17DXO3QxZ4E130_provenance.
- befree-2016 importedOn "2016-02-19" NP570008.RA2sXcvDsWpLZ17BM_lMHTzmAHXOubbKwY17DXO3QxZ4E130_provenance.