Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP484449.RA85dhc2iHGvWH0gdqJGCoDqd93_cT8Z1c3WW3Mb5lnI4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP484449.RA85dhc2iHGvWH0gdqJGCoDqd93_cT8Z1c3WW3Mb5lnI4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP484449.RA85dhc2iHGvWH0gdqJGCoDqd93_cT8Z1c3WW3Mb5lnI4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP484449.RA85dhc2iHGvWH0gdqJGCoDqd93_cT8Z1c3WW3Mb5lnI4130_provenance.
- NP484449.RA85dhc2iHGvWH0gdqJGCoDqd93_cT8Z1c3WW3Mb5lnI4130_assertion description "[A third PGRN sequence variation (R433W) was found in an FTD patient with family history of ALS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484449.RA85dhc2iHGvWH0gdqJGCoDqd93_cT8Z1c3WW3Mb5lnI4130_provenance.
- NP484449.RA85dhc2iHGvWH0gdqJGCoDqd93_cT8Z1c3WW3Mb5lnI4130_assertion evidence source_evidence_literature NP484449.RA85dhc2iHGvWH0gdqJGCoDqd93_cT8Z1c3WW3Mb5lnI4130_provenance.
- NP484449.RA85dhc2iHGvWH0gdqJGCoDqd93_cT8Z1c3WW3Mb5lnI4130_assertion SIO_000772 17202431 NP484449.RA85dhc2iHGvWH0gdqJGCoDqd93_cT8Z1c3WW3Mb5lnI4130_provenance.
- NP484449.RA85dhc2iHGvWH0gdqJGCoDqd93_cT8Z1c3WW3Mb5lnI4130_assertion wasDerivedFrom befree-20150227 NP484449.RA85dhc2iHGvWH0gdqJGCoDqd93_cT8Z1c3WW3Mb5lnI4130_provenance.
- NP484449.RA85dhc2iHGvWH0gdqJGCoDqd93_cT8Z1c3WW3Mb5lnI4130_assertion wasGeneratedBy ECO_0000203 NP484449.RA85dhc2iHGvWH0gdqJGCoDqd93_cT8Z1c3WW3Mb5lnI4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP484449.RA85dhc2iHGvWH0gdqJGCoDqd93_cT8Z1c3WW3Mb5lnI4130_provenance.