Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP822803.RAC7BcpP4T_j7JOaGH628UlxGd8EiPf4KWsfyI24zKDvU130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP822803.RAC7BcpP4T_j7JOaGH628UlxGd8EiPf4KWsfyI24zKDvU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP822803.RAC7BcpP4T_j7JOaGH628UlxGd8EiPf4KWsfyI24zKDvU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP822803.RAC7BcpP4T_j7JOaGH628UlxGd8EiPf4KWsfyI24zKDvU130_provenance.
- NP822803.RAC7BcpP4T_j7JOaGH628UlxGd8EiPf4KWsfyI24zKDvU130_assertion description "[A new locus (SPG46) maps to 9p21.2-q21.12 in a Tunisian family with a complicated autosomal recessive hereditary spastic paraplegia with mental impairment and thin corpus callosum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP822803.RAC7BcpP4T_j7JOaGH628UlxGd8EiPf4KWsfyI24zKDvU130_provenance.
- NP822803.RAC7BcpP4T_j7JOaGH628UlxGd8EiPf4KWsfyI24zKDvU130_assertion evidence source_evidence_literature NP822803.RAC7BcpP4T_j7JOaGH628UlxGd8EiPf4KWsfyI24zKDvU130_provenance.
- NP822803.RAC7BcpP4T_j7JOaGH628UlxGd8EiPf4KWsfyI24zKDvU130_assertion SIO_000772 20593214 NP822803.RAC7BcpP4T_j7JOaGH628UlxGd8EiPf4KWsfyI24zKDvU130_provenance.
- NP822803.RAC7BcpP4T_j7JOaGH628UlxGd8EiPf4KWsfyI24zKDvU130_assertion wasDerivedFrom befree-2016 NP822803.RAC7BcpP4T_j7JOaGH628UlxGd8EiPf4KWsfyI24zKDvU130_provenance.
- NP822803.RAC7BcpP4T_j7JOaGH628UlxGd8EiPf4KWsfyI24zKDvU130_assertion wasGeneratedBy ECO_0000203 NP822803.RAC7BcpP4T_j7JOaGH628UlxGd8EiPf4KWsfyI24zKDvU130_provenance.
- befree-2016 importedOn "2016-02-19" NP822803.RAC7BcpP4T_j7JOaGH628UlxGd8EiPf4KWsfyI24zKDvU130_provenance.