Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP310267.RAFX-0IxCglotb97sMs0-SRjy8C_obDBqg0RE5XQbfa6Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP310267.RAFX-0IxCglotb97sMs0-SRjy8C_obDBqg0RE5XQbfa6Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP310267.RAFX-0IxCglotb97sMs0-SRjy8C_obDBqg0RE5XQbfa6Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP310267.RAFX-0IxCglotb97sMs0-SRjy8C_obDBqg0RE5XQbfa6Q130_provenance.
- NP310267.RAFX-0IxCglotb97sMs0-SRjy8C_obDBqg0RE5XQbfa6Q130_assertion description "[The absence of a dystrophic phenotype in these mice suggests that down-regulation of ALP does not participate in facioscapulohumeral muscular dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP310267.RAFX-0IxCglotb97sMs0-SRjy8C_obDBqg0RE5XQbfa6Q130_provenance.
- NP310267.RAFX-0IxCglotb97sMs0-SRjy8C_obDBqg0RE5XQbfa6Q130_assertion evidence source_evidence_literature NP310267.RAFX-0IxCglotb97sMs0-SRjy8C_obDBqg0RE5XQbfa6Q130_provenance.
- NP310267.RAFX-0IxCglotb97sMs0-SRjy8C_obDBqg0RE5XQbfa6Q130_assertion SIO_000772 11238905 NP310267.RAFX-0IxCglotb97sMs0-SRjy8C_obDBqg0RE5XQbfa6Q130_provenance.
- NP310267.RAFX-0IxCglotb97sMs0-SRjy8C_obDBqg0RE5XQbfa6Q130_assertion wasDerivedFrom befree-2016 NP310267.RAFX-0IxCglotb97sMs0-SRjy8C_obDBqg0RE5XQbfa6Q130_provenance.
- NP310267.RAFX-0IxCglotb97sMs0-SRjy8C_obDBqg0RE5XQbfa6Q130_assertion wasGeneratedBy ECO_0000203 NP310267.RAFX-0IxCglotb97sMs0-SRjy8C_obDBqg0RE5XQbfa6Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP310267.RAFX-0IxCglotb97sMs0-SRjy8C_obDBqg0RE5XQbfa6Q130_provenance.