Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1245065.RAqPS7JijAQadY6d6VGtnwxsMWsnianaaKdqqW7kEw1m4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1245065.RAqPS7JijAQadY6d6VGtnwxsMWsnianaaKdqqW7kEw1m4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1245065.RAqPS7JijAQadY6d6VGtnwxsMWsnianaaKdqqW7kEw1m4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1245065.RAqPS7JijAQadY6d6VGtnwxsMWsnianaaKdqqW7kEw1m4130_provenance.
- NP1245065.RAqPS7JijAQadY6d6VGtnwxsMWsnianaaKdqqW7kEw1m4130_assertion description "[Our results showed that patients, homozygous for the FANCG founder mutation, present with severe cytopenia but progress to bone marrow failure at similar ages to other individuals affected with FA of heterogeneous genotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1245065.RAqPS7JijAQadY6d6VGtnwxsMWsnianaaKdqqW7kEw1m4130_provenance.
- NP1245065.RAqPS7JijAQadY6d6VGtnwxsMWsnianaaKdqqW7kEw1m4130_assertion evidence source_evidence_literature NP1245065.RAqPS7JijAQadY6d6VGtnwxsMWsnianaaKdqqW7kEw1m4130_provenance.
- NP1245065.RAqPS7JijAQadY6d6VGtnwxsMWsnianaaKdqqW7kEw1m4130_assertion SIO_000772 25477267 NP1245065.RAqPS7JijAQadY6d6VGtnwxsMWsnianaaKdqqW7kEw1m4130_provenance.
- NP1245065.RAqPS7JijAQadY6d6VGtnwxsMWsnianaaKdqqW7kEw1m4130_assertion wasDerivedFrom befree-2016 NP1245065.RAqPS7JijAQadY6d6VGtnwxsMWsnianaaKdqqW7kEw1m4130_provenance.
- NP1245065.RAqPS7JijAQadY6d6VGtnwxsMWsnianaaKdqqW7kEw1m4130_assertion wasGeneratedBy ECO_0000203 NP1245065.RAqPS7JijAQadY6d6VGtnwxsMWsnianaaKdqqW7kEw1m4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1245065.RAqPS7JijAQadY6d6VGtnwxsMWsnianaaKdqqW7kEw1m4130_provenance.