Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP690093.RAT90ibvizH8iT6hklnves5577JWV4xH297COs8b38Lww130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP690093.RAT90ibvizH8iT6hklnves5577JWV4xH297COs8b38Lww130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP690093.RAT90ibvizH8iT6hklnves5577JWV4xH297COs8b38Lww130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP690093.RAT90ibvizH8iT6hklnves5577JWV4xH297COs8b38Lww130_provenance.
- NP690093.RAT90ibvizH8iT6hklnves5577JWV4xH297COs8b38Lww130_assertion description "[A mutation scanning of exons and flanking regions of PGRN was carried out in 120 patients with sporadic frontotemporal lobar degeneration and 145 with sporadic AD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP690093.RAT90ibvizH8iT6hklnves5577JWV4xH297COs8b38Lww130_provenance.
- NP690093.RAT90ibvizH8iT6hklnves5577JWV4xH297COs8b38Lww130_assertion evidence source_evidence_literature NP690093.RAT90ibvizH8iT6hklnves5577JWV4xH297COs8b38Lww130_provenance.
- NP690093.RAT90ibvizH8iT6hklnves5577JWV4xH297COs8b38Lww130_assertion SIO_000772 18752597 NP690093.RAT90ibvizH8iT6hklnves5577JWV4xH297COs8b38Lww130_provenance.
- NP690093.RAT90ibvizH8iT6hklnves5577JWV4xH297COs8b38Lww130_assertion wasDerivedFrom befree-2016 NP690093.RAT90ibvizH8iT6hklnves5577JWV4xH297COs8b38Lww130_provenance.
- NP690093.RAT90ibvizH8iT6hklnves5577JWV4xH297COs8b38Lww130_assertion wasGeneratedBy ECO_0000203 NP690093.RAT90ibvizH8iT6hklnves5577JWV4xH297COs8b38Lww130_provenance.
- befree-2016 importedOn "2016-02-19" NP690093.RAT90ibvizH8iT6hklnves5577JWV4xH297COs8b38Lww130_provenance.