Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP592189.RAcNhcrNPXIb0A4sbDgAnXJV-U-y-bVSQVUJ8vl4ITd-4130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP592189.RAcNhcrNPXIb0A4sbDgAnXJV-U-y-bVSQVUJ8vl4ITd-4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP592189.RAcNhcrNPXIb0A4sbDgAnXJV-U-y-bVSQVUJ8vl4ITd-4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP592189.RAcNhcrNPXIb0A4sbDgAnXJV-U-y-bVSQVUJ8vl4ITd-4130_provenance.
- NP592189.RAcNhcrNPXIb0A4sbDgAnXJV-U-y-bVSQVUJ8vl4ITd-4130_assertion description "[The recent mapping of the NBS gene to chromosome 8q21 demonstrates that NBS is genetically distinct from ataxia telangiectasia (AT).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP592189.RAcNhcrNPXIb0A4sbDgAnXJV-U-y-bVSQVUJ8vl4ITd-4130_provenance.
- NP592189.RAcNhcrNPXIb0A4sbDgAnXJV-U-y-bVSQVUJ8vl4ITd-4130_assertion evidence source_evidence_literature NP592189.RAcNhcrNPXIb0A4sbDgAnXJV-U-y-bVSQVUJ8vl4ITd-4130_provenance.
- NP592189.RAcNhcrNPXIb0A4sbDgAnXJV-U-y-bVSQVUJ8vl4ITd-4130_assertion SIO_000772 9271379 NP592189.RAcNhcrNPXIb0A4sbDgAnXJV-U-y-bVSQVUJ8vl4ITd-4130_provenance.
- NP592189.RAcNhcrNPXIb0A4sbDgAnXJV-U-y-bVSQVUJ8vl4ITd-4130_assertion wasDerivedFrom befree-20150227 NP592189.RAcNhcrNPXIb0A4sbDgAnXJV-U-y-bVSQVUJ8vl4ITd-4130_provenance.
- NP592189.RAcNhcrNPXIb0A4sbDgAnXJV-U-y-bVSQVUJ8vl4ITd-4130_assertion wasGeneratedBy ECO_0000203 NP592189.RAcNhcrNPXIb0A4sbDgAnXJV-U-y-bVSQVUJ8vl4ITd-4130_provenance.
- befree-20150227 importedOn "2015-02-27" NP592189.RAcNhcrNPXIb0A4sbDgAnXJV-U-y-bVSQVUJ8vl4ITd-4130_provenance.