Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP412662.RArbbcJrV7majZoPzHI0qRRSYREbozzNa4oVFGF33q_hU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP412662.RArbbcJrV7majZoPzHI0qRRSYREbozzNa4oVFGF33q_hU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP412662.RArbbcJrV7majZoPzHI0qRRSYREbozzNa4oVFGF33q_hU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP412662.RArbbcJrV7majZoPzHI0qRRSYREbozzNa4oVFGF33q_hU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP412662.RArbbcJrV7majZoPzHI0qRRSYREbozzNa4oVFGF33q_hU130_provenance.
- NP412662.RArbbcJrV7majZoPzHI0qRRSYREbozzNa4oVFGF33q_hU130_assertion wasGeneratedBy ECO_0000203 NP412662.RArbbcJrV7majZoPzHI0qRRSYREbozzNa4oVFGF33q_hU130_provenance.
- NP412662.RArbbcJrV7majZoPzHI0qRRSYREbozzNa4oVFGF33q_hU130_assertion wasDerivedFrom befree-20150227 NP412662.RArbbcJrV7majZoPzHI0qRRSYREbozzNa4oVFGF33q_hU130_provenance.
- NP412662.RArbbcJrV7majZoPzHI0qRRSYREbozzNa4oVFGF33q_hU130_assertion SIO_000772 9034011 NP412662.RArbbcJrV7majZoPzHI0qRRSYREbozzNa4oVFGF33q_hU130_provenance.
- NP412662.RArbbcJrV7majZoPzHI0qRRSYREbozzNa4oVFGF33q_hU130_assertion evidence source_evidence_literature NP412662.RArbbcJrV7majZoPzHI0qRRSYREbozzNa4oVFGF33q_hU130_provenance.
- NP412662.RArbbcJrV7majZoPzHI0qRRSYREbozzNa4oVFGF33q_hU130_assertion description "[Data from these 2 cases are compared to analogous information from previous reports about individuals with the FRAXE or FRAXA (FMR1) mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP412662.RArbbcJrV7majZoPzHI0qRRSYREbozzNa4oVFGF33q_hU130_provenance.