Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP92436.RAZ2CW3IcT1WJhns0s9vAEdF93Bn10kvt8cVwc9zKnJg0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP92436.RAZ2CW3IcT1WJhns0s9vAEdF93Bn10kvt8cVwc9zKnJg0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP92436.RAZ2CW3IcT1WJhns0s9vAEdF93Bn10kvt8cVwc9zKnJg0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP92436.RAZ2CW3IcT1WJhns0s9vAEdF93Bn10kvt8cVwc9zKnJg0130_provenance.
- NP92436.RAZ2CW3IcT1WJhns0s9vAEdF93Bn10kvt8cVwc9zKnJg0130_assertion description "[Clinical features and molecular modelling of novel MPZ mutations in demyelinating and axonal neuropathies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP92436.RAZ2CW3IcT1WJhns0s9vAEdF93Bn10kvt8cVwc9zKnJg0130_provenance.
- NP92436.RAZ2CW3IcT1WJhns0s9vAEdF93Bn10kvt8cVwc9zKnJg0130_assertion evidence source_evidence_literature NP92436.RAZ2CW3IcT1WJhns0s9vAEdF93Bn10kvt8cVwc9zKnJg0130_provenance.
- NP92436.RAZ2CW3IcT1WJhns0s9vAEdF93Bn10kvt8cVwc9zKnJg0130_assertion SIO_000772 19293842 NP92436.RAZ2CW3IcT1WJhns0s9vAEdF93Bn10kvt8cVwc9zKnJg0130_provenance.
- NP92436.RAZ2CW3IcT1WJhns0s9vAEdF93Bn10kvt8cVwc9zKnJg0130_assertion wasDerivedFrom gad-20150221 NP92436.RAZ2CW3IcT1WJhns0s9vAEdF93Bn10kvt8cVwc9zKnJg0130_provenance.
- NP92436.RAZ2CW3IcT1WJhns0s9vAEdF93Bn10kvt8cVwc9zKnJg0130_assertion wasGeneratedBy ECO_0000203 NP92436.RAZ2CW3IcT1WJhns0s9vAEdF93Bn10kvt8cVwc9zKnJg0130_provenance.
- gad-20150221 importedOn "2015-02-21" NP92436.RAZ2CW3IcT1WJhns0s9vAEdF93Bn10kvt8cVwc9zKnJg0130_provenance.