Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP262680.RAEVC6rob1bJxuPZcEg_nQyScbiGhXioMPQxmFE9huSWU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP262680.RAEVC6rob1bJxuPZcEg_nQyScbiGhXioMPQxmFE9huSWU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP262680.RAEVC6rob1bJxuPZcEg_nQyScbiGhXioMPQxmFE9huSWU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP262680.RAEVC6rob1bJxuPZcEg_nQyScbiGhXioMPQxmFE9huSWU130_provenance.
- NP262680.RAEVC6rob1bJxuPZcEg_nQyScbiGhXioMPQxmFE9huSWU130_assertion description "[The dysferlin gene responsible for these disorders is considered a primary candidate gene for WDM.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP262680.RAEVC6rob1bJxuPZcEg_nQyScbiGhXioMPQxmFE9huSWU130_provenance.
- NP262680.RAEVC6rob1bJxuPZcEg_nQyScbiGhXioMPQxmFE9huSWU130_assertion evidence source_evidence_literature NP262680.RAEVC6rob1bJxuPZcEg_nQyScbiGhXioMPQxmFE9huSWU130_provenance.
- NP262680.RAEVC6rob1bJxuPZcEg_nQyScbiGhXioMPQxmFE9huSWU130_assertion SIO_000772 10482271 NP262680.RAEVC6rob1bJxuPZcEg_nQyScbiGhXioMPQxmFE9huSWU130_provenance.
- NP262680.RAEVC6rob1bJxuPZcEg_nQyScbiGhXioMPQxmFE9huSWU130_assertion wasDerivedFrom befree-2016 NP262680.RAEVC6rob1bJxuPZcEg_nQyScbiGhXioMPQxmFE9huSWU130_provenance.
- NP262680.RAEVC6rob1bJxuPZcEg_nQyScbiGhXioMPQxmFE9huSWU130_assertion wasGeneratedBy ECO_0000203 NP262680.RAEVC6rob1bJxuPZcEg_nQyScbiGhXioMPQxmFE9huSWU130_provenance.
- befree-2016 importedOn "2016-02-19" NP262680.RAEVC6rob1bJxuPZcEg_nQyScbiGhXioMPQxmFE9huSWU130_provenance.