Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP718733.RAlf-EGftGb_VkVNZmacSmbpa5H5GTnkZ5RrQsRTTsEeU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718733.RAlf-EGftGb_VkVNZmacSmbpa5H5GTnkZ5RrQsRTTsEeU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718733.RAlf-EGftGb_VkVNZmacSmbpa5H5GTnkZ5RrQsRTTsEeU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718733.RAlf-EGftGb_VkVNZmacSmbpa5H5GTnkZ5RrQsRTTsEeU130_provenance.
- befree-2016 importedOn "2016-02-19" NP718733.RAlf-EGftGb_VkVNZmacSmbpa5H5GTnkZ5RrQsRTTsEeU130_provenance.
- NP718733.RAlf-EGftGb_VkVNZmacSmbpa5H5GTnkZ5RrQsRTTsEeU130_assertion wasGeneratedBy ECO_0000203 NP718733.RAlf-EGftGb_VkVNZmacSmbpa5H5GTnkZ5RrQsRTTsEeU130_provenance.
- NP718733.RAlf-EGftGb_VkVNZmacSmbpa5H5GTnkZ5RrQsRTTsEeU130_assertion wasDerivedFrom befree-2016 NP718733.RAlf-EGftGb_VkVNZmacSmbpa5H5GTnkZ5RrQsRTTsEeU130_provenance.
- NP718733.RAlf-EGftGb_VkVNZmacSmbpa5H5GTnkZ5RrQsRTTsEeU130_assertion SIO_000772 19194467 NP718733.RAlf-EGftGb_VkVNZmacSmbpa5H5GTnkZ5RrQsRTTsEeU130_provenance.
- NP718733.RAlf-EGftGb_VkVNZmacSmbpa5H5GTnkZ5RrQsRTTsEeU130_assertion evidence source_evidence_literature NP718733.RAlf-EGftGb_VkVNZmacSmbpa5H5GTnkZ5RrQsRTTsEeU130_provenance.
- NP718733.RAlf-EGftGb_VkVNZmacSmbpa5H5GTnkZ5RrQsRTTsEeU130_assertion description "[In three cases (25%), MPL(W515L) was found and in two of these a combination with trisomy 21 or the Philadelphia chromosome occurred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718733.RAlf-EGftGb_VkVNZmacSmbpa5H5GTnkZ5RrQsRTTsEeU130_provenance.