Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP901680.RAv3I5XBq5MuHPuZD72HfyydmlkTEhSd3RM8dHOhjcxbM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP901680.RAv3I5XBq5MuHPuZD72HfyydmlkTEhSd3RM8dHOhjcxbM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP901680.RAv3I5XBq5MuHPuZD72HfyydmlkTEhSd3RM8dHOhjcxbM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP901680.RAv3I5XBq5MuHPuZD72HfyydmlkTEhSd3RM8dHOhjcxbM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP901680.RAv3I5XBq5MuHPuZD72HfyydmlkTEhSd3RM8dHOhjcxbM130_provenance.
- NP901680.RAv3I5XBq5MuHPuZD72HfyydmlkTEhSd3RM8dHOhjcxbM130_assertion wasGeneratedBy ECO_0000203 NP901680.RAv3I5XBq5MuHPuZD72HfyydmlkTEhSd3RM8dHOhjcxbM130_provenance.
- NP901680.RAv3I5XBq5MuHPuZD72HfyydmlkTEhSd3RM8dHOhjcxbM130_assertion wasDerivedFrom befree-20150227 NP901680.RAv3I5XBq5MuHPuZD72HfyydmlkTEhSd3RM8dHOhjcxbM130_provenance.
- NP901680.RAv3I5XBq5MuHPuZD72HfyydmlkTEhSd3RM8dHOhjcxbM130_assertion SIO_000772 19211642 NP901680.RAv3I5XBq5MuHPuZD72HfyydmlkTEhSd3RM8dHOhjcxbM130_provenance.
- NP901680.RAv3I5XBq5MuHPuZD72HfyydmlkTEhSd3RM8dHOhjcxbM130_assertion evidence source_evidence_literature NP901680.RAv3I5XBq5MuHPuZD72HfyydmlkTEhSd3RM8dHOhjcxbM130_provenance.
- NP901680.RAv3I5XBq5MuHPuZD72HfyydmlkTEhSd3RM8dHOhjcxbM130_assertion description "[Most Shwachman-Diamond syndrome patients have mutations in the SBDS gene located at chromosome 7 and suffer from recurrent infections, due to neutropenia in combination with impaired neutrophil chemotaxis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP901680.RAv3I5XBq5MuHPuZD72HfyydmlkTEhSd3RM8dHOhjcxbM130_provenance.