Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP587117.RA3pKIFTCmOgm2x-mD0JpTZTVWKYUs8uBRpK7mo8sU6sI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP587117.RA3pKIFTCmOgm2x-mD0JpTZTVWKYUs8uBRpK7mo8sU6sI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP587117.RA3pKIFTCmOgm2x-mD0JpTZTVWKYUs8uBRpK7mo8sU6sI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP587117.RA3pKIFTCmOgm2x-mD0JpTZTVWKYUs8uBRpK7mo8sU6sI130_provenance.
- NP587117.RA3pKIFTCmOgm2x-mD0JpTZTVWKYUs8uBRpK7mo8sU6sI130_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." NP587117.RA3pKIFTCmOgm2x-mD0JpTZTVWKYUs8uBRpK7mo8sU6sI130_provenance.
- NP587117.RA3pKIFTCmOgm2x-mD0JpTZTVWKYUs8uBRpK7mo8sU6sI130_assertion evidence source_evidence_literature NP587117.RA3pKIFTCmOgm2x-mD0JpTZTVWKYUs8uBRpK7mo8sU6sI130_provenance.
- NP587117.RA3pKIFTCmOgm2x-mD0JpTZTVWKYUs8uBRpK7mo8sU6sI130_assertion SIO_000772 17202431 NP587117.RA3pKIFTCmOgm2x-mD0JpTZTVWKYUs8uBRpK7mo8sU6sI130_provenance.
- NP587117.RA3pKIFTCmOgm2x-mD0JpTZTVWKYUs8uBRpK7mo8sU6sI130_assertion wasDerivedFrom befree-2016 NP587117.RA3pKIFTCmOgm2x-mD0JpTZTVWKYUs8uBRpK7mo8sU6sI130_provenance.
- NP587117.RA3pKIFTCmOgm2x-mD0JpTZTVWKYUs8uBRpK7mo8sU6sI130_assertion wasGeneratedBy ECO_0000203 NP587117.RA3pKIFTCmOgm2x-mD0JpTZTVWKYUs8uBRpK7mo8sU6sI130_provenance.
- befree-2016 importedOn "2016-02-19" NP587117.RA3pKIFTCmOgm2x-mD0JpTZTVWKYUs8uBRpK7mo8sU6sI130_provenance.