Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP487124.RA49oTR6G3jnAThp88wl37UJwCNpg5g-a_3rwGjy0H15k130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP487124.RA49oTR6G3jnAThp88wl37UJwCNpg5g-a_3rwGjy0H15k130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP487124.RA49oTR6G3jnAThp88wl37UJwCNpg5g-a_3rwGjy0H15k130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP487124.RA49oTR6G3jnAThp88wl37UJwCNpg5g-a_3rwGjy0H15k130_provenance.
- NP487124.RA49oTR6G3jnAThp88wl37UJwCNpg5g-a_3rwGjy0H15k130_assertion description "[This study describes the first COL4A4 mutation in an individual with biopsy-proven TBMD who did not have a family member with autosomal-recessive or X-linked Alport syndrome, inherited renal failure, or deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP487124.RA49oTR6G3jnAThp88wl37UJwCNpg5g-a_3rwGjy0H15k130_provenance.
- NP487124.RA49oTR6G3jnAThp88wl37UJwCNpg5g-a_3rwGjy0H15k130_assertion evidence source_evidence_literature NP487124.RA49oTR6G3jnAThp88wl37UJwCNpg5g-a_3rwGjy0H15k130_provenance.
- NP487124.RA49oTR6G3jnAThp88wl37UJwCNpg5g-a_3rwGjy0H15k130_assertion SIO_000772 11473630 NP487124.RA49oTR6G3jnAThp88wl37UJwCNpg5g-a_3rwGjy0H15k130_provenance.
- NP487124.RA49oTR6G3jnAThp88wl37UJwCNpg5g-a_3rwGjy0H15k130_assertion wasDerivedFrom befree-20140225 NP487124.RA49oTR6G3jnAThp88wl37UJwCNpg5g-a_3rwGjy0H15k130_provenance.
- NP487124.RA49oTR6G3jnAThp88wl37UJwCNpg5g-a_3rwGjy0H15k130_assertion wasGeneratedBy ECO_0000203 NP487124.RA49oTR6G3jnAThp88wl37UJwCNpg5g-a_3rwGjy0H15k130_provenance.
- befree-20140225 importedOn "2014-02-25" NP487124.RA49oTR6G3jnAThp88wl37UJwCNpg5g-a_3rwGjy0H15k130_provenance.