Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP320157.RAdWX6RDFE_RAmqOXw8Cs8OhiYm0ReV7bXAXcJJhsV53g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP320157.RAdWX6RDFE_RAmqOXw8Cs8OhiYm0ReV7bXAXcJJhsV53g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP320157.RAdWX6RDFE_RAmqOXw8Cs8OhiYm0ReV7bXAXcJJhsV53g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP320157.RAdWX6RDFE_RAmqOXw8Cs8OhiYm0ReV7bXAXcJJhsV53g130_provenance.
- NP320157.RAdWX6RDFE_RAmqOXw8Cs8OhiYm0ReV7bXAXcJJhsV53g130_assertion description "[The paternal COL4A5 mutation seems to account for the complete phenotype of ATS in the father and the maternal mutation in MYH9 for the inner ear deafness in the mother.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320157.RAdWX6RDFE_RAmqOXw8Cs8OhiYm0ReV7bXAXcJJhsV53g130_provenance.
- NP320157.RAdWX6RDFE_RAmqOXw8Cs8OhiYm0ReV7bXAXcJJhsV53g130_assertion evidence source_evidence_literature NP320157.RAdWX6RDFE_RAmqOXw8Cs8OhiYm0ReV7bXAXcJJhsV53g130_provenance.
- NP320157.RAdWX6RDFE_RAmqOXw8Cs8OhiYm0ReV7bXAXcJJhsV53g130_assertion SIO_000772 23144074 NP320157.RAdWX6RDFE_RAmqOXw8Cs8OhiYm0ReV7bXAXcJJhsV53g130_provenance.
- NP320157.RAdWX6RDFE_RAmqOXw8Cs8OhiYm0ReV7bXAXcJJhsV53g130_assertion wasDerivedFrom befree-20150227 NP320157.RAdWX6RDFE_RAmqOXw8Cs8OhiYm0ReV7bXAXcJJhsV53g130_provenance.
- NP320157.RAdWX6RDFE_RAmqOXw8Cs8OhiYm0ReV7bXAXcJJhsV53g130_assertion wasGeneratedBy ECO_0000203 NP320157.RAdWX6RDFE_RAmqOXw8Cs8OhiYm0ReV7bXAXcJJhsV53g130_provenance.
- befree-20150227 importedOn "2015-02-27" NP320157.RAdWX6RDFE_RAmqOXw8Cs8OhiYm0ReV7bXAXcJJhsV53g130_provenance.