Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP677002.RAFMrkOqzeFXCjd_REqNQ7tSl_YVWLpNu3iDmFlPJvijk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP677002.RAFMrkOqzeFXCjd_REqNQ7tSl_YVWLpNu3iDmFlPJvijk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP677002.RAFMrkOqzeFXCjd_REqNQ7tSl_YVWLpNu3iDmFlPJvijk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP677002.RAFMrkOqzeFXCjd_REqNQ7tSl_YVWLpNu3iDmFlPJvijk130_provenance.
- NP677002.RAFMrkOqzeFXCjd_REqNQ7tSl_YVWLpNu3iDmFlPJvijk130_assertion description "[These findings indicate that MHS-related RYR1 mutations may present later in life with prominent axial weakness but not always typical histopathological features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP677002.RAFMrkOqzeFXCjd_REqNQ7tSl_YVWLpNu3iDmFlPJvijk130_provenance.
- NP677002.RAFMrkOqzeFXCjd_REqNQ7tSl_YVWLpNu3iDmFlPJvijk130_assertion evidence source_evidence_literature NP677002.RAFMrkOqzeFXCjd_REqNQ7tSl_YVWLpNu3iDmFlPJvijk130_provenance.
- NP677002.RAFMrkOqzeFXCjd_REqNQ7tSl_YVWLpNu3iDmFlPJvijk130_assertion SIO_000772 23329375 NP677002.RAFMrkOqzeFXCjd_REqNQ7tSl_YVWLpNu3iDmFlPJvijk130_provenance.
- NP677002.RAFMrkOqzeFXCjd_REqNQ7tSl_YVWLpNu3iDmFlPJvijk130_assertion wasDerivedFrom befree-20150227 NP677002.RAFMrkOqzeFXCjd_REqNQ7tSl_YVWLpNu3iDmFlPJvijk130_provenance.
- NP677002.RAFMrkOqzeFXCjd_REqNQ7tSl_YVWLpNu3iDmFlPJvijk130_assertion wasGeneratedBy ECO_0000203 NP677002.RAFMrkOqzeFXCjd_REqNQ7tSl_YVWLpNu3iDmFlPJvijk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP677002.RAFMrkOqzeFXCjd_REqNQ7tSl_YVWLpNu3iDmFlPJvijk130_provenance.