Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP731544.RA_dZN7wiaK6CcuxvMxMify54w59sV9LHX2zvaHndjNUU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP731544.RA_dZN7wiaK6CcuxvMxMify54w59sV9LHX2zvaHndjNUU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP731544.RA_dZN7wiaK6CcuxvMxMify54w59sV9LHX2zvaHndjNUU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP731544.RA_dZN7wiaK6CcuxvMxMify54w59sV9LHX2zvaHndjNUU130_provenance.
- NP731544.RA_dZN7wiaK6CcuxvMxMify54w59sV9LHX2zvaHndjNUU130_assertion description "[The data suggest that different COL17A1 mutations and their combinations can result in a spectrum of biologic and clinical phenotypes of not only generalized atrophic benign epidermolysis bullosa, but also localized junctional epidermolysis bullosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP731544.RA_dZN7wiaK6CcuxvMxMify54w59sV9LHX2zvaHndjNUU130_provenance.
- NP731544.RA_dZN7wiaK6CcuxvMxMify54w59sV9LHX2zvaHndjNUU130_assertion evidence source_evidence_literature NP731544.RA_dZN7wiaK6CcuxvMxMify54w59sV9LHX2zvaHndjNUU130_provenance.
- NP731544.RA_dZN7wiaK6CcuxvMxMify54w59sV9LHX2zvaHndjNUU130_assertion SIO_000772 9740252 NP731544.RA_dZN7wiaK6CcuxvMxMify54w59sV9LHX2zvaHndjNUU130_provenance.
- NP731544.RA_dZN7wiaK6CcuxvMxMify54w59sV9LHX2zvaHndjNUU130_assertion wasDerivedFrom befree-20140225 NP731544.RA_dZN7wiaK6CcuxvMxMify54w59sV9LHX2zvaHndjNUU130_provenance.
- NP731544.RA_dZN7wiaK6CcuxvMxMify54w59sV9LHX2zvaHndjNUU130_assertion wasGeneratedBy ECO_0000203 NP731544.RA_dZN7wiaK6CcuxvMxMify54w59sV9LHX2zvaHndjNUU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP731544.RA_dZN7wiaK6CcuxvMxMify54w59sV9LHX2zvaHndjNUU130_provenance.