Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP715399.RApY6_C6houg_TY4i6nFxD7WUo4Ck0_kMeiEdlmsXhunQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP715399.RApY6_C6houg_TY4i6nFxD7WUo4Ck0_kMeiEdlmsXhunQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP715399.RApY6_C6houg_TY4i6nFxD7WUo4Ck0_kMeiEdlmsXhunQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP715399.RApY6_C6houg_TY4i6nFxD7WUo4Ck0_kMeiEdlmsXhunQ130_provenance.
- NP715399.RApY6_C6houg_TY4i6nFxD7WUo4Ck0_kMeiEdlmsXhunQ130_assertion description "[In a population-based study from Western Sweden MLPA was used to determine the copy-numbers of several genes in the SMA region (SMN1, SMN2, BIRC1, GTF2H2 and SERF1A) in SMA-patients and their parents.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP715399.RApY6_C6houg_TY4i6nFxD7WUo4Ck0_kMeiEdlmsXhunQ130_provenance.
- NP715399.RApY6_C6houg_TY4i6nFxD7WUo4Ck0_kMeiEdlmsXhunQ130_assertion evidence source_evidence_literature NP715399.RApY6_C6houg_TY4i6nFxD7WUo4Ck0_kMeiEdlmsXhunQ130_provenance.
- NP715399.RApY6_C6houg_TY4i6nFxD7WUo4Ck0_kMeiEdlmsXhunQ130_assertion SIO_000772 19154529 NP715399.RApY6_C6houg_TY4i6nFxD7WUo4Ck0_kMeiEdlmsXhunQ130_provenance.
- NP715399.RApY6_C6houg_TY4i6nFxD7WUo4Ck0_kMeiEdlmsXhunQ130_assertion wasDerivedFrom befree-2016 NP715399.RApY6_C6houg_TY4i6nFxD7WUo4Ck0_kMeiEdlmsXhunQ130_provenance.
- NP715399.RApY6_C6houg_TY4i6nFxD7WUo4Ck0_kMeiEdlmsXhunQ130_assertion wasGeneratedBy ECO_0000203 NP715399.RApY6_C6houg_TY4i6nFxD7WUo4Ck0_kMeiEdlmsXhunQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP715399.RApY6_C6houg_TY4i6nFxD7WUo4Ck0_kMeiEdlmsXhunQ130_provenance.