Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_provenance.
- NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_assertion description "[L1 syndrome and X-linked NDI are distinct clinical disorders caused by mutations in the L1CAM and AVPR2 genes, respectively, located in adjacent positions in Xq28.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_provenance.
- NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_assertion evidence source_evidence_literature NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_provenance.
- NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_assertion SIO_000772 18553546 NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_provenance.
- NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_assertion wasDerivedFrom befree-20150227 NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_provenance.
- NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_assertion wasGeneratedBy ECO_0000203 NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP768633.RAsJ4JYsNOdfMEjI11tEeWt0Q2Q9TUfs-FYGsWJ17Ug1g130_provenance.