Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP452088.RA0XmCph0yDwZ_LbAQ_4TrgQgVgtLH7RVrR49Ks6Sq99g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP452088.RA0XmCph0yDwZ_LbAQ_4TrgQgVgtLH7RVrR49Ks6Sq99g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP452088.RA0XmCph0yDwZ_LbAQ_4TrgQgVgtLH7RVrR49Ks6Sq99g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP452088.RA0XmCph0yDwZ_LbAQ_4TrgQgVgtLH7RVrR49Ks6Sq99g130_provenance.
- NP452088.RA0XmCph0yDwZ_LbAQ_4TrgQgVgtLH7RVrR49Ks6Sq99g130_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." NP452088.RA0XmCph0yDwZ_LbAQ_4TrgQgVgtLH7RVrR49Ks6Sq99g130_provenance.
- NP452088.RA0XmCph0yDwZ_LbAQ_4TrgQgVgtLH7RVrR49Ks6Sq99g130_assertion evidence source_evidence_literature NP452088.RA0XmCph0yDwZ_LbAQ_4TrgQgVgtLH7RVrR49Ks6Sq99g130_provenance.
- NP452088.RA0XmCph0yDwZ_LbAQ_4TrgQgVgtLH7RVrR49Ks6Sq99g130_assertion SIO_000772 23329375 NP452088.RA0XmCph0yDwZ_LbAQ_4TrgQgVgtLH7RVrR49Ks6Sq99g130_provenance.
- NP452088.RA0XmCph0yDwZ_LbAQ_4TrgQgVgtLH7RVrR49Ks6Sq99g130_assertion wasDerivedFrom befree-20140225 NP452088.RA0XmCph0yDwZ_LbAQ_4TrgQgVgtLH7RVrR49Ks6Sq99g130_provenance.
- NP452088.RA0XmCph0yDwZ_LbAQ_4TrgQgVgtLH7RVrR49Ks6Sq99g130_assertion wasGeneratedBy ECO_0000203 NP452088.RA0XmCph0yDwZ_LbAQ_4TrgQgVgtLH7RVrR49Ks6Sq99g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP452088.RA0XmCph0yDwZ_LbAQ_4TrgQgVgtLH7RVrR49Ks6Sq99g130_provenance.