Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP251028.RAoVG0IIOucQgnJ8Ixe3DnWDAJnvCYsiRhWuuyHH2U9sk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP251028.RAoVG0IIOucQgnJ8Ixe3DnWDAJnvCYsiRhWuuyHH2U9sk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP251028.RAoVG0IIOucQgnJ8Ixe3DnWDAJnvCYsiRhWuuyHH2U9sk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP251028.RAoVG0IIOucQgnJ8Ixe3DnWDAJnvCYsiRhWuuyHH2U9sk130_provenance.
- NP251028.RAoVG0IIOucQgnJ8Ixe3DnWDAJnvCYsiRhWuuyHH2U9sk130_assertion description "[Snyder-Robinson syndrome (SRS, OMIM 309583) is a rare X-linked syndrome characterized by mental retardation, marfanoid habitus, skeletal defects, osteoporosis, and facial asymmetry.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP251028.RAoVG0IIOucQgnJ8Ixe3DnWDAJnvCYsiRhWuuyHH2U9sk130_provenance.
- NP251028.RAoVG0IIOucQgnJ8Ixe3DnWDAJnvCYsiRhWuuyHH2U9sk130_assertion evidence source_evidence_literature NP251028.RAoVG0IIOucQgnJ8Ixe3DnWDAJnvCYsiRhWuuyHH2U9sk130_provenance.
- NP251028.RAoVG0IIOucQgnJ8Ixe3DnWDAJnvCYsiRhWuuyHH2U9sk130_assertion SIO_000772 19206178 NP251028.RAoVG0IIOucQgnJ8Ixe3DnWDAJnvCYsiRhWuuyHH2U9sk130_provenance.
- NP251028.RAoVG0IIOucQgnJ8Ixe3DnWDAJnvCYsiRhWuuyHH2U9sk130_assertion wasDerivedFrom befree-20140225 NP251028.RAoVG0IIOucQgnJ8Ixe3DnWDAJnvCYsiRhWuuyHH2U9sk130_provenance.
- NP251028.RAoVG0IIOucQgnJ8Ixe3DnWDAJnvCYsiRhWuuyHH2U9sk130_assertion wasGeneratedBy ECO_0000203 NP251028.RAoVG0IIOucQgnJ8Ixe3DnWDAJnvCYsiRhWuuyHH2U9sk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP251028.RAoVG0IIOucQgnJ8Ixe3DnWDAJnvCYsiRhWuuyHH2U9sk130_provenance.