Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1020655.RAj849fllb12MzPf6rKdCpEu5o9zmujJ9eP5MlK7p6o4Q130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1020655.RAj849fllb12MzPf6rKdCpEu5o9zmujJ9eP5MlK7p6o4Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1020655.RAj849fllb12MzPf6rKdCpEu5o9zmujJ9eP5MlK7p6o4Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1020655.RAj849fllb12MzPf6rKdCpEu5o9zmujJ9eP5MlK7p6o4Q130_provenance.
- NP1020655.RAj849fllb12MzPf6rKdCpEu5o9zmujJ9eP5MlK7p6o4Q130_assertion description "[Mutations in multidomain protein MEGF8 identify a Carpenter syndrome subtype associated with defective lateralization.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1020655.RAj849fllb12MzPf6rKdCpEu5o9zmujJ9eP5MlK7p6o4Q130_provenance.
- NP1020655.RAj849fllb12MzPf6rKdCpEu5o9zmujJ9eP5MlK7p6o4Q130_assertion evidence source_evidence_literature NP1020655.RAj849fllb12MzPf6rKdCpEu5o9zmujJ9eP5MlK7p6o4Q130_provenance.
- NP1020655.RAj849fllb12MzPf6rKdCpEu5o9zmujJ9eP5MlK7p6o4Q130_assertion SIO_000772 23063620 NP1020655.RAj849fllb12MzPf6rKdCpEu5o9zmujJ9eP5MlK7p6o4Q130_provenance.
- NP1020655.RAj849fllb12MzPf6rKdCpEu5o9zmujJ9eP5MlK7p6o4Q130_assertion wasDerivedFrom befree-2016 NP1020655.RAj849fllb12MzPf6rKdCpEu5o9zmujJ9eP5MlK7p6o4Q130_provenance.
- NP1020655.RAj849fllb12MzPf6rKdCpEu5o9zmujJ9eP5MlK7p6o4Q130_assertion wasGeneratedBy ECO_0000203 NP1020655.RAj849fllb12MzPf6rKdCpEu5o9zmujJ9eP5MlK7p6o4Q130_provenance.
- befree-2016 importedOn "2016-02-19" NP1020655.RAj849fllb12MzPf6rKdCpEu5o9zmujJ9eP5MlK7p6o4Q130_provenance.