Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP343195.RAJtTnzAR3CkAYi1adkitE0GEeIJ0oO5nRnuB39ivqb0w130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP343195.RAJtTnzAR3CkAYi1adkitE0GEeIJ0oO5nRnuB39ivqb0w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP343195.RAJtTnzAR3CkAYi1adkitE0GEeIJ0oO5nRnuB39ivqb0w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP343195.RAJtTnzAR3CkAYi1adkitE0GEeIJ0oO5nRnuB39ivqb0w130_provenance.
- NP343195.RAJtTnzAR3CkAYi1adkitE0GEeIJ0oO5nRnuB39ivqb0w130_assertion description "[Our findings expand the molecular, cellular, and clinical spectrum of HPS-2 and call for an increased index of suspicion for this diagnosis among patients with features of albinism, bleeding, and neutropenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP343195.RAJtTnzAR3CkAYi1adkitE0GEeIJ0oO5nRnuB39ivqb0w130_provenance.
- NP343195.RAJtTnzAR3CkAYi1adkitE0GEeIJ0oO5nRnuB39ivqb0w130_assertion evidence source_evidence_literature NP343195.RAJtTnzAR3CkAYi1adkitE0GEeIJ0oO5nRnuB39ivqb0w130_provenance.
- NP343195.RAJtTnzAR3CkAYi1adkitE0GEeIJ0oO5nRnuB39ivqb0w130_assertion SIO_000772 11809908 NP343195.RAJtTnzAR3CkAYi1adkitE0GEeIJ0oO5nRnuB39ivqb0w130_provenance.
- NP343195.RAJtTnzAR3CkAYi1adkitE0GEeIJ0oO5nRnuB39ivqb0w130_assertion wasDerivedFrom befree-2016 NP343195.RAJtTnzAR3CkAYi1adkitE0GEeIJ0oO5nRnuB39ivqb0w130_provenance.
- NP343195.RAJtTnzAR3CkAYi1adkitE0GEeIJ0oO5nRnuB39ivqb0w130_assertion wasGeneratedBy ECO_0000203 NP343195.RAJtTnzAR3CkAYi1adkitE0GEeIJ0oO5nRnuB39ivqb0w130_provenance.
- befree-2016 importedOn "2016-02-19" NP343195.RAJtTnzAR3CkAYi1adkitE0GEeIJ0oO5nRnuB39ivqb0w130_provenance.