Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP541049.RAJOi20R3xnbiPk1unq-VD-dQxhW5Qmv87VgBO1OwmphU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP541049.RAJOi20R3xnbiPk1unq-VD-dQxhW5Qmv87VgBO1OwmphU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP541049.RAJOi20R3xnbiPk1unq-VD-dQxhW5Qmv87VgBO1OwmphU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP541049.RAJOi20R3xnbiPk1unq-VD-dQxhW5Qmv87VgBO1OwmphU130_provenance.
- NP541049.RAJOi20R3xnbiPk1unq-VD-dQxhW5Qmv87VgBO1OwmphU130_assertion description "[Recently, mutations in Latent Transforming Growth Factor (TGF)-beta Binding Protein 2 (LTBP2) have been reported in several families that were diagnosed with PCG, who actually had a more complex ocular phenotype with ectopia lentis and Marfanoid features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541049.RAJOi20R3xnbiPk1unq-VD-dQxhW5Qmv87VgBO1OwmphU130_provenance.
- NP541049.RAJOi20R3xnbiPk1unq-VD-dQxhW5Qmv87VgBO1OwmphU130_assertion evidence source_evidence_literature NP541049.RAJOi20R3xnbiPk1unq-VD-dQxhW5Qmv87VgBO1OwmphU130_provenance.
- NP541049.RAJOi20R3xnbiPk1unq-VD-dQxhW5Qmv87VgBO1OwmphU130_assertion SIO_000772 22924778 NP541049.RAJOi20R3xnbiPk1unq-VD-dQxhW5Qmv87VgBO1OwmphU130_provenance.
- NP541049.RAJOi20R3xnbiPk1unq-VD-dQxhW5Qmv87VgBO1OwmphU130_assertion wasDerivedFrom befree-20150227 NP541049.RAJOi20R3xnbiPk1unq-VD-dQxhW5Qmv87VgBO1OwmphU130_provenance.
- NP541049.RAJOi20R3xnbiPk1unq-VD-dQxhW5Qmv87VgBO1OwmphU130_assertion wasGeneratedBy ECO_0000203 NP541049.RAJOi20R3xnbiPk1unq-VD-dQxhW5Qmv87VgBO1OwmphU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP541049.RAJOi20R3xnbiPk1unq-VD-dQxhW5Qmv87VgBO1OwmphU130_provenance.