Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP222933.RAlv4mKVFmXi8XSW1iAo7ylV6X1DaktYmM3Ia9c2ydYSk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP222933.RAlv4mKVFmXi8XSW1iAo7ylV6X1DaktYmM3Ia9c2ydYSk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP222933.RAlv4mKVFmXi8XSW1iAo7ylV6X1DaktYmM3Ia9c2ydYSk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP222933.RAlv4mKVFmXi8XSW1iAo7ylV6X1DaktYmM3Ia9c2ydYSk130_provenance.
- NP222933.RAlv4mKVFmXi8XSW1iAo7ylV6X1DaktYmM3Ia9c2ydYSk130_assertion description "[Whole-exome sequencing identifies ADAM10 mutations as a cause of reticulate acropigmentation of Kitamura, a clinical entity distinct from Dowling-Degos disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP222933.RAlv4mKVFmXi8XSW1iAo7ylV6X1DaktYmM3Ia9c2ydYSk130_provenance.
- NP222933.RAlv4mKVFmXi8XSW1iAo7ylV6X1DaktYmM3Ia9c2ydYSk130_assertion evidence source_evidence_literature NP222933.RAlv4mKVFmXi8XSW1iAo7ylV6X1DaktYmM3Ia9c2ydYSk130_provenance.
- NP222933.RAlv4mKVFmXi8XSW1iAo7ylV6X1DaktYmM3Ia9c2ydYSk130_assertion SIO_000772 23666529 NP222933.RAlv4mKVFmXi8XSW1iAo7ylV6X1DaktYmM3Ia9c2ydYSk130_provenance.
- NP222933.RAlv4mKVFmXi8XSW1iAo7ylV6X1DaktYmM3Ia9c2ydYSk130_assertion wasDerivedFrom befree-20150227 NP222933.RAlv4mKVFmXi8XSW1iAo7ylV6X1DaktYmM3Ia9c2ydYSk130_provenance.
- NP222933.RAlv4mKVFmXi8XSW1iAo7ylV6X1DaktYmM3Ia9c2ydYSk130_assertion wasGeneratedBy ECO_0000203 NP222933.RAlv4mKVFmXi8XSW1iAo7ylV6X1DaktYmM3Ia9c2ydYSk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP222933.RAlv4mKVFmXi8XSW1iAo7ylV6X1DaktYmM3Ia9c2ydYSk130_provenance.