Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP861371.RANKu0bdnjPiz1Z8ZlzyKmTxgc8Zhzu677eBplSZLbgcc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP861371.RANKu0bdnjPiz1Z8ZlzyKmTxgc8Zhzu677eBplSZLbgcc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP861371.RANKu0bdnjPiz1Z8ZlzyKmTxgc8Zhzu677eBplSZLbgcc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP861371.RANKu0bdnjPiz1Z8ZlzyKmTxgc8Zhzu677eBplSZLbgcc130_provenance.
- NP861371.RANKu0bdnjPiz1Z8ZlzyKmTxgc8Zhzu677eBplSZLbgcc130_assertion description "[Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP861371.RANKu0bdnjPiz1Z8ZlzyKmTxgc8Zhzu677eBplSZLbgcc130_provenance.
- NP861371.RANKu0bdnjPiz1Z8ZlzyKmTxgc8Zhzu677eBplSZLbgcc130_assertion evidence source_evidence_literature NP861371.RANKu0bdnjPiz1Z8ZlzyKmTxgc8Zhzu677eBplSZLbgcc130_provenance.
- NP861371.RANKu0bdnjPiz1Z8ZlzyKmTxgc8Zhzu677eBplSZLbgcc130_assertion SIO_000772 16813530 NP861371.RANKu0bdnjPiz1Z8ZlzyKmTxgc8Zhzu677eBplSZLbgcc130_provenance.
- NP861371.RANKu0bdnjPiz1Z8ZlzyKmTxgc8Zhzu677eBplSZLbgcc130_assertion wasDerivedFrom befree-20140225 NP861371.RANKu0bdnjPiz1Z8ZlzyKmTxgc8Zhzu677eBplSZLbgcc130_provenance.
- NP861371.RANKu0bdnjPiz1Z8ZlzyKmTxgc8Zhzu677eBplSZLbgcc130_assertion wasGeneratedBy ECO_0000203 NP861371.RANKu0bdnjPiz1Z8ZlzyKmTxgc8Zhzu677eBplSZLbgcc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP861371.RANKu0bdnjPiz1Z8ZlzyKmTxgc8Zhzu677eBplSZLbgcc130_provenance.